14936-67-5 Usage
General Description
1-methyldecyl acetate is a chemical compound that belongs to the class of organic esters. It is composed of a 1-methyldecyl group, which consists of 10 carbon atoms in a straight chain with a methyl (CH3) group attached at the first carbon, and an acetate group. It is commonly used as a flavoring agent in foods and beverages due to its fruity and sweet aroma. Additionally, 1-methyldecyl acetate is used in various industrial applications, including the production of fragrances, perfumes, and cosmetics. It is also used as a solvent in cleaning products and as a component in adhesive formulations. Overall, 1-methyldecyl acetate is a versatile chemical with a wide range of practical and commercial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 14936-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,3 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14936-67:
(7*1)+(6*4)+(5*9)+(4*3)+(3*6)+(2*6)+(1*7)=125
125 % 10 = 5
So 14936-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H26O2/c1-4-5-6-7-8-9-10-11-12(2)15-13(3)14/h12H,4-11H2,1-3H3
14936-67-5Relevant articles and documents
Lentinus strigellus: a new versatile stereoselective biocatalyst for the bioreduction of prochiral ketones
Barros-Filho, Bartholomeu A.,de Oliveira, Maria da Conceicao F.,Lemos, Telma L.G.,de Mattos, Marcos C.,Gonzalo, Gonzalo de,Gotor-Fernandez, Vicente,Gotor, Vicente
experimental part, p. 1057 - 1061 (2009/10/02)
Growing cells of the basiodiomycete Lentinus strigellus in potato-dextrose broth have been used for the first time as a biocatalyst in the stereoselective reduction of aromatic and aliphatic ketones. Most of the aromatic ketones were converted into the corresponding optically active alcohols in up to >99% enantiomeric excess under very mild reaction conditions. Among the aliphatic ketones tested, 2-octanone was enzymatically reduced by this microorganism to enantiopure (S)-2-octanol with almost complete conversion.
