1787-09-3 Usage
Description
(1E)-1-Hexadecenyl acetate, also known as hexadecenyl acetate, is a colorless liquid with a sweet, floral odor. It belongs to the class of organic compounds known as long-chain fatty acids and derivatives. This chemical compound is commonly found in natural sources such as fruits, vegetables, and flowers.
Uses
Used in Fragrance and Flavor Industry:
(1E)-1-Hexadecenyl acetate is used as a fragrance and flavoring agent for its pleasant scent. It is commonly used in the formulation of perfumes, soaps, and other cosmetic products.
Used in Insect Repellent Industry:
(1E)-1-Hexadecenyl acetate is used as an ingredient in some insect repellents due to its potential insecticidal and repellent properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1787-09-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1787-09:
(6*1)+(5*7)+(4*8)+(3*7)+(2*0)+(1*9)=103
103 % 10 = 3
So 1787-09-3 is a valid CAS Registry Number.
1787-09-3Relevant articles and documents
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Craig,J.C. et al.
, p. 907 - 910 (1965)
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Synthesis and properties of natural occurring α-hydroxyaldehydes
Kern, Werner,Spiteller, Gerhard
, p. 4347 - 4362 (2007/10/03)
A synthesis for aliphatic α-acetoxyaldehydes 18 is presented. These were converted to free aldehydes 9 by action of hog liver esterase. Aliphatic α-hydroxyaldehydes, recently recognized to be produced in the course of lipid-peroxidation of linoleic and other unsaturated fatty acids, are only stable for short time in solution. They react with amines to give Schiff bases. These are instable, but can be trapped after reduction with NaBH4 to the corresponding amines. Since α-hydroxyaldehydes are produced in the case of lipid peroxidation and were found to stimulate oxidative stress, Schiff base formation might be a physiological important process. α-Hydroxyaldehydes form under physiological conditions mercaptals by reaction with thiols.