2719-27-9 Usage
Description
Cyclohexanecarboxylic acid chloride, also known as cyclohexanecarbonyl chloride, is a chemical compound derived from cyclohexanecarboxylic acid. It is a clear, colorless to straw-colored liquid with various applications in different industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid chloride is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to form derivatives with potential therapeutic applications makes it a valuable component in drug development.
Used in Chemical Synthesis:
In the chemical industry, cyclohexanecarboxylic acid chloride is utilized as a versatile reagent for the preparation of various organic compounds. Its electrochemical reduction at a hanging mercury drop electrode in acetonitrile has been reported, showcasing its potential in chemical reactions and synthesis processes.
Used in Agricultural Industry:
Cyclohexanecarboxylic acid chloride is used as a precursor in the preparation of five thiourea derivative ligands with anti-bacterial and anti-yeast activity. These ligands include N-(diethylcarbamothioyl)cyclohexanecarboxamide, N-(di-n-propylcarbamothioyl)cyclohexanecarboxamide, di-n-butylcarbamothioyl)cyclohexanecarboxamide, N-(diphenylcarbamothioyl)cyclohexanecarboxamide, and N-(morpholine-4-carbonothioyl)cyclohexanecarboxamide. These compounds have potential applications in the development of new anti-bacterial and anti-yeast agents for agricultural use, contributing to the control of plant diseases and improving crop yields.
Check Digit Verification of cas no
The CAS Registry Mumber 2719-27-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2719-27:
(6*2)+(5*7)+(4*1)+(3*9)+(2*2)+(1*7)=89
89 % 10 = 9
So 2719-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H11ClO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2
2719-27-9Relevant articles and documents
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Thaler
, p. 4370 (1968)
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Rhodium(III)-catalyzed chemodivergent annulations between phenyloxazoles and diazos via C–H activation
Zhang, Xueguo,Wang, Peigen,Zhu, Liangwei,Chen, Baohua
supporting information, p. 695 - 699 (2020/06/28)
Acid-controlled, chemodivergent and redox-neutral annulations for the synthesis of isocoumarins and isoquinolinones have been realized via Rh(III)-catalyzed C[sbnd]H activation. Diazo compounds act as a carbene precursor, and coupling occurs in one-pot process, where adipic acid and trimethylacetic acid promote chemodivergent cyclizations.
Decarboxylative Borylation of mCPBA-Activated Aliphatic Acids
Wei, Dian,Liu, Tu-Ming,Zhou, Bo,Han, Bing
supporting information, p. 234 - 238 (2020/01/02)
A decarboxylative borylation of aliphatic acids for the synthesis of a variety of alkylboronates has been developed by mixing m-chloroperoxybenzoic acid (mCPBA)-activated fatty acids with bis(catecholato)diboron in N,N-dimethylformamide (DMF) at room temperature. A radical chain process is involved in the reaction which initiates from the B-B bond homolysis followed by the radical transfer from the boron atom to the carbon atom with subsequent decarboxylation and borylation.