Cas no 76023-99-9 ((1R-cis)-Cyhalothric Acid)

(1R-cis)-Cyhalothric Acid is a stereospecific isomer of cyhalothric acid, notable for its high purity and selective biological activity. As a key intermediate in the synthesis of pyrethroid insecticides, its cis-configuration ensures enhanced efficacy in pest control applications. The compound exhibits superior stability and reactivity, making it valuable for precision chemical formulations. Its well-defined stereochemistry allows for targeted interactions with biological systems, reducing off-target effects. (1R-cis)-Cyhalothric Acid is commonly utilized in agricultural and pharmaceutical research due to its consistent performance and compatibility with synthetic processes. Proper handling and storage are essential to maintain its integrity and functionality.
(1R-cis)-Cyhalothric Acid structure
(1R-cis)-Cyhalothric Acid structure
Product Name:(1R-cis)-Cyhalothric Acid
CAS No:76023-99-9
MF:C9H10ClF3O2
MW:242.622712612152
CID:4658580
Update Time:2025-10-22

(1R-cis)-Cyhalothric Acid Chemical and Physical Properties

Names and Identifiers

    • (1R-cis)-Cyhalothric Acid
    • Inchi: 1S/C9H10ClF3O2/c1-8(2)4(6(8)7(14)15)3-5(10)9(11,12)13/h3-4,6H,1-2H3,(H,14,15)/b5-3-/t4-,6-/m0/s1
    • InChI Key: SPVZAYWHHVLPBN-WREUKLMHSA-N
    • SMILES: [C@@H]1(C(O)=O)[C@H](/C=C(\Cl)/C(F)(F)F)C1(C)C

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Additional information on (1R-cis)-Cyhalothric Acid

Comprehensive Analysis of (1R-cis)-Cyhalothric Acid (CAS No. 76023-99-9): Properties, Applications, and Industry Insights

(1R-cis)-Cyhalothric Acid (CAS No. 76023-99-9) is a stereospecific isomer of cyhalothric acid, a compound widely studied in the field of organic chemistry and agrochemical research. Its unique cis-configuration and chirality make it a subject of interest for researchers exploring enantioselective synthesis and bioactive molecule development. The compound's molecular structure, characterized by a cyclopropane ring and carboxyl group, contributes to its stability and reactivity under controlled conditions.

In recent years, the demand for chiral intermediates like (1R-cis)-Cyhalothric Acid has surged due to advancements in asymmetric catalysis and green chemistry. Industry professionals frequently search for terms such as "stereoselective synthesis methods" or "CAS 76023-99-9 applications," reflecting the compound's relevance in pharmaceutical and agricultural innovation. Analytical techniques such as HPLC and NMR spectroscopy are commonly employed to verify its purity and stereochemical integrity.

The environmental fate of (1R-cis)-Cyhalothric Acid has also garnered attention, with studies focusing on its biodegradation pathways and ecotoxicological profile. Regulatory agencies emphasize the importance of sustainable chemical practices, aligning with global trends toward eco-friendly agrochemicals. Researchers often investigate its metabolite formation and soil adsorption properties to assess environmental compatibility.

From a commercial perspective, CAS 76023-99-9 is utilized in the development of high-performance crop protection agents. Its efficacy as a synergistic component in formulations has been documented in peer-reviewed journals, addressing common queries like "how to enhance pesticide selectivity" or "role of chiral compounds in agriculture." Manufacturers prioritize cost-effective synthesis routes to meet market demands while adhering to Good Manufacturing Practices (GMP).

Emerging technologies such as computational chemistry and AI-driven molecular modeling are revolutionizing the study of (1R-cis)-Cyhalothric Acid. These tools enable predictive analyses of its reaction mechanisms and molecular interactions, topics frequently searched by academic and industrial chemists. Collaborative efforts between academia and enterprises aim to optimize its large-scale production while minimizing waste generation.

Quality control remains paramount for CAS 76023-99-9, with specifications including ≥98% purity and strict enantiomeric excess (ee) standards. Analytical certificates often highlight parameters like melting point and optical rotation, critical for end-users in R&D. Storage recommendations typically suggest anhydrous conditions and low-temperature preservation to maintain stability.

In conclusion, (1R-cis)-Cyhalothric Acid exemplifies the intersection of chiral chemistry and applied sciences. Its multifaceted applications—from agrochemicals to methodological research—underscore its significance in modern chemistry. As industries increasingly prioritize stereochemical precision and sustainability, this compound will likely remain a focal point for innovation and optimization.

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