70813-65-9 Usage
Description
Ethyl 10-chlorodecanoate is an organochlorine ester compound formed by the reaction of an alcohol with a carboxylic acid. It is characterized by the presence of a chlorine atom in its molecule, which may have implications for its toxicity and environmental impact. This chemical compound is known for its pleasant odor and unique chemical properties, making it a versatile ingredient in various industries.
Uses
Used in Cosmetics and Perfumery Industry:
Ethyl 10-chlorodecanoate is used as a fragrance ingredient for its pleasant odor, contributing to the scent profiles of various cosmetic and perfume products.
Used in Pharmaceutical Industry:
Ethyl 10-chlorodecanoate is used as a solvent in certain pharmaceutical formulations, aiding in the dissolution and delivery of active ingredients.
Used in Chemical and Material Development:
Due to its unique chemical properties, ethyl 10-chlorodecanoate may have potential applications in the development of new materials and chemicals, although further research is needed to explore these possibilities.
However, it is important to carefully consider the potential health and environmental effects of ethyl 10-chlorodecanoate before its widespread use, as organochlorine compounds are known to have certain risks associated with them.
Check Digit Verification of cas no
The CAS Registry Mumber 70813-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,1 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70813-65:
(7*7)+(6*0)+(5*8)+(4*1)+(3*3)+(2*6)+(1*5)=119
119 % 10 = 9
So 70813-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H23ClO2/c1-2-15-12(14)10-8-6-4-3-5-7-9-11-13/h2-11H2,1H3
70813-65-9Relevant articles and documents
Process for the monoalkylation of C-H acid methylene groups
-
Page/Page column 6, (2008/06/13)
The ratio of the alkali(ne earth) carbonate to the methylene group-containing substrate is above 0.6 : 1 in the monoalkylation of C-H acid methylene groups by reaction of the substrate in a polar aprotic solvent with a dihalogen compound having its halogens separated by a chain of at least3C and with reaction being in presence of the alkali(ne earth) carbonates and a phase transfer catalyst and being accompanied by continuous removal of the water formed. An Independent claim is also included for production of omega-haloalkyl-nitriles or -carboxylic acids by reacting a malonic acid diester or cyanoacetic ester with an alpha,omega-dihaloalkane as above and then saponifying and decarboxylating the product.
