766-92-7 Usage
Description
BENZYL METHYL SULFIDE is an organic compound that occurs naturally in cooked pork. It is a clear, colorless to pale yellow liquid with a distinctive sulfur-containing aroma. Its chemical structure consists of a benzyl group attached to a methyl sulfide group, which contributes to its unique properties and potential applications.
Uses
Used in Flavor and Fragrance Industry:
BENZYL METHYL SULFIDE is used as a flavoring agent for its characteristic sulfur-containing aroma. It is employed in the development of food products, particularly those with a savory or meaty taste, to enhance their flavor profile and provide a more authentic and appetizing experience for consumers.
Used in Pharmaceutical Industry:
BENZYL METHYL SULFIDE is used as a building block or intermediate in the synthesis of various pharmaceutical compounds. Its sulfur-containing structure allows it to be a versatile component in the development of drugs with potential therapeutic applications.
Used in Chemical Research:
BENZYL METHYL SULFIDE serves as a valuable research tool in organic chemistry, particularly in the study of sulfur-containing compounds and their reactions. It can be used to investigate the reactivity, stability, and properties of sulfur-containing molecules, contributing to the advancement of chemical knowledge and the development of new compounds with potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 766-92-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 766-92:
(5*7)+(4*6)+(3*6)+(2*9)+(1*2)=97
97 % 10 = 7
So 766-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H10S/c1-9-7-8-5-3-2-4-6-8/h2-6H,7H2,1H3
766-92-7Relevant articles and documents
An efficient and catalyst free methylthiolation of 4-(bromomethyl)-2H-chromen-2-ones with DMSO
Chougala, Bahubali M.,Samundeeswari,Holiyachi, Megharaja,Naik, Nirmala S.,Shastri, Lokesh A.,Sunagar, Vinay A
, p. 874 - 879 (2017)
The first simple, metal free, and efficient protocol has been established for the methylthiolation of structurally diverse 4-bromomethyl-2H-chromen-2-ones using dimethyl sulfoxide (DMSO) as methylthiolation source at higher temperature. The experimental m
A nickel-catalyzed silylation reaction of alkyl aryl sulfoxides with silylzinc reagents
Li, Wei-Ze,Wang, Zhong-Xia
supporting information, p. 5082 - 5086 (2021/06/21)
Ni(PEt3)Cl2-catalyzed silylation of alkyl aryl sulfoxides with silylzinc reagents was carried out. This protocol allows alkyl aryl sulfoxides to convert to arylsilicon compounds under mild reaction conditions, tolerates a range of functional groups and is suitable for a wide scope of substrates.
Nucleophilic Amination and Etherification of Aryl Alkyl Thioethers
Wang, Xia,Tang, Yue,Long, Cheng-Yu,Dong, Wen-Ke,Li, Chenchen,Xu, Xinhua,Zhao, Wanxiang,Wang, Xue-Qiang
supporting information, p. 4749 - 4753 (2018/08/23)
A transition-metal-free protocol capable of synthesizing diarylated aniline derivatives is reported. This method could be further employed to prepare aryl alkyl ethers. A wide range of thioethers, anilines, as well as alcohols were tolerated thanks to the mild reaction conditions. The strength of our method was demonstrated by performing a gram-scale reaction (20 mmol) followed by conversion of the nitrile group into synthetically useful aldehyde, ketone, and carboxylic acid.