7476-81-5 Usage
Description
(4-chlorophenyl) butanoate, also known as ethyl 4-chlorophenylbutanoate, is a chemical compound belonging to the family of butanoate esters. It is a colorless to pale yellow liquid with a sweet, floral odor and is soluble in alcohol and oils.
Uses
Used in Food and Beverage Industry:
(4-chlorophenyl) butanoate is used as a fragrance and flavoring agent for its sweet, floral scent and taste, enhancing the aroma and flavor of various food products.
Used in Perfume and Cosmetic Industry:
(4-chlorophenyl) butanoate is used as a fragrance ingredient in the production of perfumes and cosmetics, providing a pleasant and attractive scent.
Used in Pharmaceutical Industry:
(4-chlorophenyl) butanoate is used in the manufacturing of pharmaceuticals, contributing to the development of various medicinal products.
Used in Industrial Applications:
(4-chlorophenyl) butanoate is utilized in other industrial applications, such as the production of certain chemicals and materials.
It is important to handle (4-chlorophenyl) butanoate with care, as it can be harmful if it comes into contact with the skin or is ingested.
Check Digit Verification of cas no
The CAS Registry Mumber 7476-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7476-81:
(6*7)+(5*4)+(4*7)+(3*6)+(2*8)+(1*1)=125
125 % 10 = 5
So 7476-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-2-3-10(12)13-9-6-4-8(11)5-7-9/h4-7H,2-3H2,1H3
7476-81-5Relevant articles and documents
Enzymatic resolution, desymmetrization, and dynamic kinetic asymmetric transformation of 1,3-cycloalkanediols
Fransson, Ann-Britt L.,Xu, Yongmei,Leijondahl, Karin,Baeckvall, Jan-E.
, p. 6309 - 6316 (2007/10/03)
An efficient desymmetrization of cis-1,3-cyclohexanediol to (1S,3R)-3-(acetoxy)-1-cyclohexanol ((R,S)-2a) was performed via Candida antarctica lipase B (CALB)-catalyzed transesterification, in high yield (up to 93%) and excellent enantioselectivity (ee's