1918-88-3 Usage
Description
[(3-methylbutyl)sulfinyl]benzene, with the molecular formula C11H16OS, is a sulfur-containing organic compound belonging to the benzene derivatives family. It is naturally found in vegetables like garlic, onion, and leek, contributing to their distinct aroma and flavor. [(3-methylbutyl)sulfinyl]benzene has been studied for its potential health benefits, which include antimicrobial, antioxidant, and anti-inflammatory properties. Furthermore, it has been investigated for its possible role in cancer prevention and treatment. Its unique chemical structure and biological activities make it a subject of interest for research and development in various sectors, such as food science, medicine, and agriculture.
Uses
Used in Food Industry:
[(3-methylbutyl)sulfinyl]benzene is used as a flavoring agent for its characteristic aroma, enhancing the taste and smell of various food products.
Used in Pharmaceutical Industry:
[(3-methylbutyl)sulfinyl]benzene is used as a potential therapeutic agent for its antimicrobial, antioxidant, and anti-inflammatory properties, which can contribute to the development of new drugs for various health conditions.
Used in Agricultural Industry:
[(3-methylbutyl)sulfinyl]benzene is used as a natural pesticide due to its antimicrobial properties, which can help protect crops from diseases and pests.
Used in Cancer Research:
[(3-methylbutyl)sulfinyl]benzene is used as a subject of study in cancer prevention and treatment, with its potential health benefits being explored for the development of novel cancer therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 1918-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1918-88:
(6*1)+(5*9)+(4*1)+(3*8)+(2*8)+(1*8)=103
103 % 10 = 3
So 1918-88-3 is a valid CAS Registry Number.
1918-88-3Relevant 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.).
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.
CONJUGATE ADDITION OF ALKYL GROUPS TO α,β-UNSATURATED SULFOXIDES VIA MICHAEL ADDITION OF NITROPARAFFINS AND SUBSEQUENT DENITRATION WITH TRIBUTYLTIN HYDRIDE
Ono, Noboru,Miyake, Hideyoshi,Kamimura, Akio,Tsukui, Nobuo,Kaji, Aritsune
, p. 2957 - 2960 (2007/10/02)
Michael addition of nitroparaffins to α,β-unsaturated sulfoxides is well effected in the presence of DBU.The nitro group in the adduct is replaced by hydrogen with Bu3SnH without influence to the sulfinyl function.The overall reactions provide an efficien
