1787-09-3 Usage
General Description
(1E)-1-Hexadecenyl acetate, also known as hexadecenyl acetate, is a chemical compound that belongs to the class of organic compounds known as long-chain fatty acids and derivatives. It is a colorless liquid with a sweet, floral odor that is commonly used in the fragrance and flavor industry. Hexadecenyl acetate can be found in various natural sources such as fruits, vegetables, and flowers. It is often used in the formulation of perfumes, soaps, and other cosmetic products due to its pleasant scent. Additionally, it has been reported to have potential insecticidal and repellent properties, making it an ingredient in some insect repellents.
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.
