13910-11-7 Usage
Description
[(3-methylbutyl)sulfanyl]benzene, also known as 4-tert-butylthiobenzene, is an organic compound characterized by its molecular formula C11H16S. It features a benzene ring with a thioether group at the 4-position and a tert-butyl group attached to the sulfur. This colorless to pale yellow liquid has a strong, unpleasant odor and is recognized for its stability and non-reactivity under normal conditions.
Uses
Used in Fragrance Industry:
[(3-methylbutyl)sulfanyl]benzene is used as a scent and flavoring agent for its distinct aromatic properties, contributing to the creation of various fragrances and enhancing the sensory experience of products in the fragrance industry.
Used in Food Industry:
Similarly, in the food industry, [(3-methylbutyl)sulfanyl]benzene serves as a flavoring agent, adding unique taste and aroma to different food products, thereby improving their overall appeal to consumers.
Used in Chemical Synthesis:
[(3-methylbutyl)sulfanyl]benzene also functions as an intermediate in the synthesis of other organic compounds, playing a crucial role in the development of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 13910-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,1 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13910-11:
(7*1)+(6*3)+(5*9)+(4*1)+(3*0)+(2*1)+(1*1)=77
77 % 10 = 7
So 13910-11-7 is a valid CAS Registry Number.
13910-11-7Relevant articles and documents
An Iodine-Mediated Hofmann-L?ffler-Freytag Reaction of Sulfoximines Leading to Dihydroisothiazole Oxides
Zhang, Duo,Wang, Han,Cheng, Hanchao,Hernández, José G.,Bolm, Carsten
supporting information, p. 4274 - 4277 (2017/10/23)
A Hofmann-L?ffler-Freytag type cyclization reaction of S-aryl-S-phenylpropyl sulfoximines (and related derivatives) was developed. Using molecular iodine as the initiator under visible light a series of five-membered cyclic products was obtained in moderate to high yields. The approach represents a new strategy for the synthesis of dihydroisothiazole oxides and benzo[d]isothiazoles-1-oxides. (Figure presented.).
Preparation of (2E,6E)-10,11-dihydrofamesol via a (bisphenyl)dithioacetal reduction
Mechelke, Mark F.,Wiemer, David F.
, p. 9609 - 9612 (2007/10/03)
Reduction of a (bisphenyl)dithioacetal with sodium/isopropyl alcohol in THF allows preparation of (2E,6E)-10,11-dihydrofarnesol in high yield.
α-Fluorination of methyl phenyl sulfoxide and related compounds by molecular fluorine: A novel method for the introduction of fluorine into sulfoxides bearing α-H atoms
Toyota, Akemi,Ono, Yoshinori,Chiba, Jun,Sugihara, Takumichi,Kaneko, Chikara
, p. 703 - 708 (2007/10/03)
Direct formation of α-fluorosulfones from sulfoxides bearing α-H atoms merely by reaction with molecular fluorine (5% F2/N2) is reported, and a novel non-Pummerer-type mechanism is proposed for this α-fluorination reaction.
