70813-65-9 Usage
General Description
Ethyl 10-chlorodecanoate is a chemical compound that is commonly used in the production of various products such as cosmetics, perfumes, and pharmaceuticals. It is an ester, which means it is formed by the reaction of an alcohol with a carboxylic acid. The presence of a chlorine atom in the molecule makes it an organochlorine compound, which may have implications for its toxicity and environmental impact. Ethyl 10-chlorodecanoate is often used as a fragrance ingredient due to its pleasant odor, and it can also function as a solvent in certain formulations. Additionally, it may have potential applications in the development of new materials and chemicals due to its unique chemical properties. However, the potential health and environmental effects of ethyl 10-chlorodecanoate should be carefully considered before its widespread use.
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
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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.
