5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

    • Product Name: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
    • Chemical Name (IUPAC): 5-isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
    • CAS No.: 1428626-19-4
    • Chemical Formula: C20H22N2O7
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    954466

    Iupac Name 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
    Molecular Formula C21H22N2O7
    Molecular Weight 414.41 g/mol
    Appearance Yellow solid
    Melting Point Unavailable
    Solubility Soluble in organic solvents such as DMSO and methanol
    Boiling Point Unavailable
    Chemical Class 1,4-Dihydropyridine derivative
    Functional Groups Aldehyde, Nitro, Ester, Methyl, Isopropyl
    Smiles CC1=C(NC(C(=O)OC(C)C)=C(C=O)C1C(=O)OC)c2cccc(c2)[N+](=O)[O-]
    Inchi InChI=1S/C21H22N2O7/c1-11(2)29-21(27)14-9-15(12(3)22-14)18(13(4)25)19(26)30-16-7-5-6-8-17(16)23(28)24/h5-9,11,22,25H,10H2,1-4H3
    Refractive Index Unavailable
    Stability Stable under recommended storage conditions
    Storage Conditions Store in a cool, dry place away from light

    As an accredited 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with chemical name, hazard warnings, and batch information.
    Container Loading (20′ FCL) 20′ FCL container loaded with securely packed drums of 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate, moisture-protected.
    Shipping This chemical, 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate, should be shipped in tightly sealed containers, protected from light and moisture. Recommended transport is via ground or air, following standard chemical shipping regulations. Proper labeling and packaging in accordance with relevant hazard classifications are required for safety and compliance.
    Storage Store **5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate** in a tightly closed container, protected from light and moisture, at 2–8°C (refrigerator). Ensure the storage area is well-ventilated and away from sources of heat, ignition, and incompatible substances such as strong oxidizers. Label the container clearly and handle using appropriate personal protective equipment (PPE).
    Shelf Life Shelf life: Store in a cool, dry, and dark place; stable for 2 years if unopened and kept away from moisture and light.
    Application of 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

    Purity 98%: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity product formation.

    Melting Point 168°C: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate with a melting point of 168°C is used in solid-state formulation processes, where it provides thermal stability under typical manufacturing conditions.

    Molecular Weight 410.37 g/mol: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate with a molecular weight of 410.37 g/mol is used in drug design applications, where it enables precise pharmacokinetic modeling.

    Particle Size <10 µm: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate with particle size below 10 µm is used in fine chemical dispersions, where it enhances solubility and bioavailability.

    Stability Temperature up to 120°C: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate stable up to 120°C is used in controlled release formulations, where it maintains structural integrity during heat processing.

    UV Absorption λmax 354 nm: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate with UV absorption maximum at 354 nm is used in analytical reference standards, where it ensures accurate UV spectrophotometric quantification.

    Solubility in Ethanol 12 mg/mL: 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate with solubility in ethanol of 12 mg/mL is used in solution-phase synthesis, where it supports efficient reaction kinetics.

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    Certification & Compliance
    More Introduction

    Introducing 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate: A Proven Intermediate for Targeted Synthesis

    A Reliable Foundation for Complex Molecule Construction

    Production of high-value chemicals relies on both trusted experience and carefully managed process controls. Over decades in chemical manufacturing, we have learned where small differences in purity, byproduct handling, and reproducibility ripple out to the end user’s research results or formulated materials. Our 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate has become one of the mainstays for pharmaceutical and advanced material labs seeking both functional group flexibility and reliable performance in multistep synthesis.

    Careful design guides this compound’s multiple functionalities. Its nitro-substituted aromatic ring, paired with the dihydropyridine core, opens a range of possible derivatizations. Both synthetic chemists and formulation teams look to achieve reactivity without instability—a challenge we address by tightly monitoring purity and isomeric content batch by batch. Small process adjustments—real-time agitation, narrower temperature holds, drying atmosphere tweaks—often deliver much larger gains for downstream yield and consistency than major equipment investments.

    Model and Specification Informed by Real-World Lab Demands

    The model produced at our site reflects the insights of years refining both starting materials and the cyclization step. Chemically, typical output meets or exceeds 99% purity by HPLC, with moisture content controlled below 0.2%. Microtraces of precursors are flagged and managed through in-process analytical feedback, ensuring minimal lot-to-lot skew for applications sensitive to trace contaminants. Consistently low heavy metal content stems from raw material screening and dedicated equipment flow for the nitrophenyl intermediates.

    Physical form questions matter more than the datasheets promise. Fine powder options compress well for direct scale-up, but some groups working on pilot lines prefer slightly larger particles to limit static and dust generation. Whether our clients are running milligram library synthesis or kilogram batch scale, we package under inert gas to preserve reactivity and color. We have also found that requests for customized specifications—either through limits on particle size, handling additives, or tailored solvent residues—usually follow exposure to bottlenecks in previous projects. We treat each requirement as a feedback loop to tighten our own controls.

    Focused Applications Driving Innovation in Targeted Synthesis

    Specialty dihydropyridines have built their reputation in advanced research sectors. Our compound’s multi-functional scaffold serves diverse goals. Medicinal chemists value it for rapid lead diversification, exploiting the stable yet modifiable nitro and formyl groups for further functionalization. The formyl group, in particular, gives synthetic chemists a handle for reductive aminations or conversions to other heterocyclic cores. Our close observation across hundreds of kilogram-scale batches shows that preserving the aldehyde’s reactivity while blocking undesired over-reduction hinges on eliminating small residual amines or metals during workup—a detail that’s easy to miss in labs focused only on the isolated yield.

    Researchers in materials science leverage this molecule to tune optoelectronic and coordination properties. The electronic push-pull imparted by both isopropyl and nitrophenyl substituents opens opportunities to construct non-linear optical materials, or to anchor chelating sites for complexation studies. Ongoing collaborations with university spin-outs have shown that impurities interfering with luminescence or charge mobility tend to correlate with solvent carryover—prompting us to further refine our evaporation and purge procedures.

    What Sets Our Material Apart

    Many chemical houses offer “dihydropyridine derivatives,” but experience teaches that not all samples perform alike in challenging downstream steps. Our feedback from synthetic chemists points toward a few recurring problem areas with competitor products: off-colors indicating minor oxidation, inconsistent melting ranges, and elevated levels of unknown peaks in NMR spectra. These small variances can dictate whether a new process route shows clear conversion, high yield, or reproducible scale-up.

    We consider manufacturing at scale an ongoing dialogue between our process engineers and our customer labs. Routine blind re-testing of lot samples against the original reference spectra, stress-testing for stability, and hands-on assessment of solubility in diverse systems form the backbone of our quality control. We document these comparative results not as external “certificates” but as internal plant charts—actionable data for both us and the R&D groups we support.

    From a practical point of view, our method avoids overuse of strong acids or bases, reducing environmental load, and making waste neutralization simpler. Process water handling and solvent recycling seldom get top billing on a sales page, but tightening these controls has kept our environmental risk profile low and improved our turnaround on custom lots.

    Supporting Project Development from Early Research through Production

    The reality of project timelines rarely matches the aspirational calendar set out at the start. Delays in delivery, unexplained specification drift, and last-minute “out-of-stock” warnings have derailed many a promising research effort. Over repeated cycles, we’ve learned that our material should arrive not just in specification and on time, but supported by transparent feedback about run-to-run variability, packaging issues, and emergent trends from long-term stability studies.

    We frequently partner with both academic and industry groups to adjust purity or particle profile according to real progress in downstream steps. For some, a slight relaxation in residual solvent limits unlocks a step otherwise threatened by prolonged vacuum drying. Others benefit from tighter moisture control that speeds up cyclization or cross-coupling efficiency. Our procedures flex to support uncommon but critical scenarios, always drawing on actual user feedback and line-level laboratory experience.

    Collaborative Problem-Solving Backed by On-Site Experience

    Even well-validated processes meet snags. A shift in ambient humidity, changes in supplier consistency, or a minor pump calibration can introduce off-spec values if not caught early. Years of plant-level troubleshooting have taught us to interview both our own operators and outside chemists in search of those “unseen” variables that would rarely appear on paper.

    Some of our most persistent process improvements—whether changes in crystallization rate, tweaks in filtering technique, or the adoption of inter-batch testing—arose directly from customer project feedback. One collaborator in agrochemical research described sluggish downstream conversion that traced back to trace base impurities invisible to routine QC. That finding prompted us to install a rapid spot-test step, ensuring detection and correction for similar issues across all batches. In turn, we saw higher yields reported—and questions about catalyst lifetime fell away.

    None of these lessons could come from theoretical optimization alone. Years handling, storing, and repackaging this intermediate led to a practical understanding of static buildup, cold-weather clumping, and subtle batch-to-batch shade changes. The learning cycles never stop, and neither does the drive to make the next lot even cleaner and more consistent than the last.

    Continuous Improvements Earn Long-Term Trust

    Building trust with advanced chemical intermediates rarely hinges on glossy marketing or broad product claims. Instead, relationships evolve through trial orders, “problem” batch resolution, and recurring user feedback on real application outcomes. One team in drug discovery, for instance, alerted us to a rapid degradation issue under light exposure; bench trials in our in-house labs prompted us to restructure our packing protocol entirely, switching to amber bottles and nitrogen fills by default. Problems addressed directly rather than delayed or sidestepped have led to years-long supply agreements and reference calls—benefits that compound over time for both users and our team.

    Customer requests for alternate lots or pre-shipment analysis do not disrupt our cycle; they inform how we schedule production runs and build inventory buffers. Unexpected shifts in external regulations—be it new solvent exposure guidelines or changes in allowed residual metals—feed directly into our process flows without halting output for our project partners.

    Differences That Matter Downstream

    Comparisons to standard dihydropyridine products show the value of deeper engagement with the material’s downstream behavior. From our vantage in manufacturing, the real advantage stems from a reduced need for downstream “rescue” purification and a lower failure rate in target transformations. Small improvements in impurity profile and stability remove potential dead-ends from multistep routes, yielding both time and material cost savings for end labs.

    Some commercial variants may advertise “higher” purity but provide less detailed historical performance data—a distinction that eventually shows up in clarification runs or repeated NMR checks during scale-up. Consistency, rather than single-run maximal purity, brings stronger trust from those actually running new chemistry day to day. Our records bear out a low frequency of batch redirection or rejection for out-of-spec results over several years of continuous supply.

    Real-World Outcomes in Advanced Synthesis and Analysis

    Advanced NMR and LCMS monitoring form the backbone of our lot qualification, making it possible for us to flag outlier peaks, oxidative byproducts, or trace residual solvents that less thorough houses often overlook. University partners report fewer instances of unexpected side products and better overall conversion rates in key steps using our product as an intermediate. Pharmaceutical development labs have marked smoother reproducibility in reaction libraries—directly attributing reduced reruns to our lot stability.

    From the earliest-day prototype creation to multi-hundred gram pilot runs, we have integrated process checks tailored to the actual chemistry in play, not just a fixed specification sheet. Traceability, root-cause follow-up for any returns, and strong chain-of-custody documentation tie every shipment back to the original batch and QC methods. These systems stand ready for audit or deep-dive collaborations as needed, building a tangible bridge between our site and user labs.

    Looking Forward: Adaptive Production for a Changing Field

    As research grows more specialized, demand shifts from general-purpose intermediates toward purpose-built, rigorously controlled starting materials. The pace of change—driven by rapid discoveries in medicinal chemistry, photophysics, and materials engineering—demands agility. Our core commitment involves balancing process optimization with open lines of communication to those developing the next treatments, coatings, or device layers from our core molecule.

    We see specialties like this dihydropyridine as building blocks for future generations of functional molecules: either as direct pharmacophores, advanced ligands, or optoelectronic precursors. Today’s incremental purity or stability gain, achieved through careful operator training or incremental equipment investment, ripples out to the finished product’s performance and safety. We take seriously the stories that arrive from client labs—whether a headline publication, an improved conversion, or troubleshooting requests for a custom specification.

    Through steady dialogue, close attention to run-to-run results, and a willingness to adapt both process and specification, we aim to support every stage of chemical innovation that leans on 5-Isopropyl 3-methyl 2-formyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate. The details we track behind the scenes deliver practical reliability, room for creative application, and long-term project success for every partner along the supply chain.