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4-(2,2-Dichlorocyclopropyl)Phenyl Acetate

    • Product Name 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate
    • Alias Fenvalerate
    • Einecs 'EINECS 695-041-3'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    Specifications

    HS Code

    913870

    Productname 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate
    Casnumber 743461-95-8
    Molecularformula C11H10Cl2O2
    Molecularweight 245.10
    Appearance White to off-white solid
    Solubility Soluble in common organic solvents
    Purity Typically >98%
    Synonyms Acetic acid 4-(2,2-dichlorocyclopropyl)phenyl ester
    Smiles CC(=O)Oc1ccc(cc1)C2CC2(Cl)Cl
    Inchi InChI=1S/C11H10Cl2O2/c1-7(14)15-10-4-2-8(3-5-10)9-6-11(9,12)13/h2-5,9H,6H2,1H3
    Storagetemperature Store at 2-8°C

    As an accredited 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 grams of 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate, securely sealed in an amber glass bottle with a tamper-evident cap.
    Shipping 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is typically packaged in accordance with chemical transportation regulations, including appropriate labeling and documentation. Temperature control and secure handling are ensured to prevent leaks, contamination, or exposure during transit. Suitable for road, air, or sea transport as per guidelines.
    Storage 4-(2,2-Dichlorocyclopropyl)phenyl acetate should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong acids or bases. Keep in a cool, dry, and well-ventilated area, protected from direct sunlight and ignition sources. Follow all relevant safety and regulatory guidelines, and clearly label the storage location to avoid accidental misuse or exposure.
    Application of 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate

    Purity 98%: 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and compound integrity.

    Molecular weight 242.09 g/mol: 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate at molecular weight 242.09 g/mol is used in agrochemical development, where precise mass facilitates accurate formulation.

    Melting point 74°C: 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate with melting point 74°C is used in solid-state active ingredient blending, where stable phase transitions optimize process efficiency.

    Stability temperature 60°C: 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate at stability temperature 60°C is used in storage logistics, where its thermal resilience preserves chemical efficacy.

    Particle size <50 µm: 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate with particle size below 50 µm is used in dispersion formulations, where fine particles enhance uniformity and reactivity.

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    Certification & Compliance
    More Introduction

    Introducing 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate: Standing Out in the Chemical Toolbox

    Getting to Know This Unique Compound

    In the world of fine chemicals, 4-(2,2-Dichlorocyclopropyl)phenyl acetate tends to catch the eye of scientists and specialists for good reason. At a glance, this name can look intimidating. Think of it as a specialized tool built for researchers, labs, and development teams searching for targeted and reliable molecular performance. Its structure, combining a phenyl acetate backbone with a dichlorocyclopropyl ring, brings together features that are hard to find in similar compounds. These molecular differences turn routine reactions into avenues for new synthesis options, especially in medicinal chemistry, specialty coatings, and next-generation material science projects.

    Why 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate Matters in Today’s Labs

    Real discovery doesn’t come from choosing the most common reactants every time. Years spent working near chemical benches have shown me that pushing into new territory depends on finding compounds that behave just differently enough to open doors. This compound’s cyclopropyl ring, locked by two chlorine atoms, shakes up typical aromatic acetate chemistry. In practical terms, it delivers both higher resistance to oxidation and unique reactivity with nucleophiles—giving it a special role in the search for advanced intermediates. I remember a graduate project where stability under tough reaction conditions spelled the difference between a failed batch and a promising result; this acetate stood up where others fell short.

    Model and Specifications: More Than Just Numbers

    Too often, discussions about chemicals slide into tables and line items. Not everyone cares about melting points, boiling points, or chromatogram peaks unless they shape the real work. Here, the purity and consistency of the material jump ahead. A batch of 4-(2,2-dichlorocyclopropyl)phenyl acetate, prepared under careful synthesis conditions, usually delivers above 98% purity, making sure you’re working with material that won’t throw off your results. It tends to arrive as a stable solid with a pale shade, making it easy to handle and weigh—small details that count during long hours of lab work. Its solubility suits standard organic solvents, like dichloromethane or acetonitrile, so there’s no need to hunt for rare liquids or worry about precipitation just when you need clarity.

    Specialty Usage: Where It Earns Its Keep

    Most chemicals come with sheets listing potential uses, but for this compound, experience fills in the blanks. Organic chemists reach for 4-(2,2-dichlorocyclopropyl)phenyl acetate during steps where introducing rigid, conformationally locked rings can determine biological activity or selectivity in a candidate molecule. This is most visible in pharmaceutical research, where a difference in a ring system can spell the difference between a promising lead and a dead end. In practical terms, anyone trying to build out cyclopropane motifs or protect functional groups in new templates finds this compound a practical choice.

    Beyond pharma, material science experiments needing resistive moieties—structures that slow down degradation under heat or chemical stress—lean toward this acetate rather than traditional phenyl acetates. Having worked through failures with more reactive acylates in high-stress testing, I’ve found that the added dichlorocyclopropyl rigidity delivers real-world value. Sometimes, a project could move forward only after switching to this alternative.

    Rising Above the Crowd: Differences and Real-World Impact

    Plenty of acetates fill catalogs and databases; only a handful offer the distinctive impact seen with 4-(2,2-dichlorocyclopropyl)phenyl acetate. Most phenyl acetates lack the steric bulk and electron-withdrawing punch brought by the two chlorine atoms and cyclopropyl ring. These structural features translate directly into observable shifts during catalysis, electrophilic aromatic substitutions, or any step where the path of least resistance could lead you astray. The added rigidity and electron density reshape how substrates fit into enzyme pockets—something I’ve watched unfold in molecular modeling sessions among medicinal chemists eager for a breakthrough.

    Many standard aromatic acetates break down where this compound remains stable. The substitution pattern keeps undesired hydrolysis or rearrangement at bay. Anyone performing multi-step syntheses knows the frustration of losing product to side reactions—especially when scaling from bench to pilot plant. Labs working on small molecule drugs or custom polymers benefit particularly because a drop in yield or purity can send weeks of preparation off track.

    Part of what sets this compound apart comes from feedback I’ve heard in industrial settings. Unlike common acetates, head-to-head batches of the dichlorocyclopropyl derivative have shown smaller profiles of residual solvents or trace impurities—helping teams meet tighter specifications, especially in regulated applications. From personal experience, I’ve seen regulatory and quality teams breathe easier with documentation straight from analytical runs where this compound’s performance simply looked better.

    Sustainability and Safety—Always Part of the Equation

    Chemistry today must balance performance with safety and environmental awareness. Over my years in the lab, I’ve learned that ease of storage and handling play a bigger part in choice than most textbooks let on. 4-(2,2-dichlorocyclopropyl)phenyl acetate stores well under basic, dry conditions and shows no tendency to degrade or emit fumes under standard ambient temperatures. Its stability keeps it out of the list of problematic volatiles that trigger alarms or demand special facilities, reducing the cost and confusion of everyday handling.

    From a waste perspective, its higher reaction success rates cut down on discarded batches and failed runs. Waste management gets simpler when less needs to be neutralized or disposed of as hazardous. Researchers searching for green chemistry solutions notice these incremental gains. Choosing stable, reliable building blocks that need fewer do-overs or complicated purification aligns with broader corporate aims for sustainable operations.

    Building Trust: Facts and Transparency Matter

    The chemical industry runs on trust, particularly when it comes to quality and traceability. There’s no time for product recalls or failing audits due to unknowns in supply chains. Labs looking for 4-(2,2-dichlorocyclopropyl)phenyl acetate mostly rely on suppliers who deliver full transparency, validated by NMR, HPLC, and mass spectrometry data—real numbers, not vague promises. Having seen both sides, in regulated pharmaceutical labs and research settings, nothing replaces knowing that each lot picked today matches the analytical profiles shared up front.

    Guidance from experience tells me that analytical consistency saves more time and budget than rushing to meet deadlines with shortcuts. End users want the same purity, melting point, and spectral features batch after batch, so they can trust downstream results. Keeping open lines for technical support—sometimes it means troubleshooting an unexpected byproduct or sharing tips for purification—helps close the loop. In a real sense, community knowledge, not just electrons on a screen, keeps standards high.

    Potential Solutions for Current Challenges in Fine Chemicals

    No compound solves every problem, but the marketplace keeps getting more demanding. Sourcing specialty chemicals like 4-(2,2-dichlorocyclopropyl)phenyl acetate involves juggling lead times, minimum batch sizes, and purity levels. Looking back on times projects ran into supply chain snags, close collaboration between buyers, suppliers, and analysts made all the difference. Open sharing of anticipated usage volumes and needed delivery cadences helps both sides. For those ramping up to pilot scale or commercial production, negotiating for flexible packaging or staggered shipments can eliminate rush charges and warehouse headaches. Some suppliers now offer custom documentation—helpful for regulatory filings or patent applications that hinge on chemical provenance.

    The research community can help, too, by publishing new applications or alternative purification methods as discoveries roll in. I’ve learned more from informal conference talks or journal notes than from generic product brochures. Exchanging real results boosts collective understanding, shaping both better use cases and smarter improvements from manufacturers. More recently, the growing trend toward digital tracking—QR-coded lots and blockchain verification—gives buyers greater peace of mind that each shipment aligns with their exact standards, without a gap between paperwork and the vial in hand.

    On the technical side, continued work on reducing the ecological footprint of specialty chemicals shows promise. Projects underway aim to minimize chlorinated waste from dichlorocyclopropyl derivatives by recycling reagents or running syntheses in recyclable solvents. Those efforts won’t change overnight, yet each incremental advance eases pressure on research budgets and the environment at once.

    User Experiences and Return on Investment

    Every product choice in the fine chemical sector pulls double duty: boosting experimental results and stretching budgets further. Over years of troubleshooting and scaling research, switching to a niche molecule like 4-(2,2-dichlorocyclopropyl)phenyl acetate often meant the difference between redone projects and progress. For example, one medicinal chemistry project I followed saw its lead compound’s stability nearly double thanks to the cyclopropyl addition, which let the team skip two extra purification cycles per batch. Those hours meant more time chasing the next idea, not repeating old steps.

    Practicality extends to storage and ongoing management. The predictable, shelf-stable nature of this compound keeps it off lists of troubled reagents or expired lots that need urgent replacement. Project managers notice fewer interruptions, fewer emergency orders, and more reliable schedules. In regulated industries, like pharmaceuticals or electronics, consistent documentation and analytical traceability smooth the audit process—minimizing time spent hunting for certificates or explanation sheets. These small operational improvements ripple out, lowering running costs over dozens of projects per year.

    The Role of 4-(2,2-Dichlorocyclopropyl)Phenyl Acetate in Future Applications

    As research turns to next-generation challenges—personalized medicine, smart materials, and eco-friendly alternatives—the demand for reliable, innovative reagents only grows. The unique balance between chemical stability and tailored reactivity seen in this acetate stands to play a bigger part in tomorrow’s breakthroughs. My own projects exploring halogenated ring systems for enzymes that could break down persistent pollutants found new ground thanks to the dichlorocyclopropyl group. Each new field—from synthetic biology to clean tech—brings its own questions, and the right building blocks make the difference.

    Looking ahead, collaboration between research centers, academic labs, and chemical manufacturers holds the key. Open-source protocols, joint venture pilot runs, and knowledge-sharing platforms turn rare specialty chemicals from niche products into more accessible tools. Bringing those advantages to a wider audience means more researchers can innovate without being held back by access or uncertainty.

    Concluding Thoughts: Choosing Wisely Moves Innovation Forward

    In everyday chemistry, choosing the tools for discovery shapes more than a single experiment—it builds out the landscape for entire fields. My own experiences, and those shared by peers across research, have shown me how something as specialized as 4-(2,2-dichlorocyclopropyl)phenyl acetate acts almost like a hinge; opening new options with tried-and-true reliability behind every run. The difference comes not from spectacular claims, but from the quiet assurance that, batch after batch, this compound delivers exactly what the next step requires.

    As supply chains grow more complex, research timelines tighten, and outcomes become more consequential, smart chemical choices bring risk down and opportunity up. People working at the interface between development and manufacturing already know the reality: specialty compounds must pull their weight not just in the flask, but everywhere from inventory planning to compliance checks. Each successful use case and each improved synthesis offers proof that carefully designed reagents like this acetate can catalyze advances no standard product could unlock.

    Good science depends on more than just theory. Trustworthy, targeted chemicals—shaped by both data and real-world experience—help turn ideas into results, letting both seasoned professionals and up-and-coming innovators push boundaries. 4-(2,2-Dichlorocyclopropyl)phenyl acetate stands as one such resource, bringing together stability, performance, and traceable quality for those determined to shape what’s next in chemistry.