6937-97-9 Usage
Description
[(prop-2-en-1-ylsulfanyl)methyl]benzene, with the molecular formula C10H12S, is a chemical compound derived from benzene. It features a propenylsulfanyl methyl group attached to the benzene ring, which contributes to its diverse applications in the chemical industry.
Uses
Used in Pharmaceutical Synthesis:
[(prop-2-en-1-ylsulfanyl)methyl]benzene is used as a precursor in the pharmaceutical industry for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of pharmaceuticals, making it a valuable starting material in drug development.
Used in Pesticide Production:
In the agricultural sector, [(prop-2-en-1-ylsulfanyl)methyl]benzene serves as a starting material for the production of pesticides. Its chemical properties enable the development of effective compounds to protect crops from pests and diseases.
Used in Organic Compound Synthesis:
[(prop-2-en-1-ylsulfanyl)methyl]benzene is also utilized in the synthesis of other organic compounds across various industries. Its versatility as a building block allows for the creation of a broad spectrum of products, from specialty chemicals to advanced materials.
Safety Precautions:
Given its flammable nature and potential health hazards, [(prop-2-en-1-ylsulfanyl)methyl]benzene should be handled with care and in a well-ventilated area to ensure the safety of those working with it. Proper handling protocols and safety measures should be followed to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6937-97-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6937-97:
(6*6)+(5*9)+(4*3)+(3*7)+(2*9)+(1*7)=139
139 % 10 = 9
So 6937-97-9 is a valid CAS Registry Number.
6937-97-9Relevant articles and documents
Sulfur ylides generated from the reaction of adamantylidene and phenylcarbene with sulfur substrates
Romashin, Yuri N.,Liu, Michael T. H.,Hill, Brian T.,Platz, Matthew S.
, p. 6519 - 6521 (2003)
Reaction of adamantylidene and phenylcarbene with ethylthiol, ethylene dithiol, allylethylsulfide, allylphenylsulfide, and trimethylenesulfide involves the formation of a sulfur ylide intermediate, followed by H-migration, 2,3-sigmatropic shift, or ring opening to give sulfides. The sulfur ylide formed in the reaction of phenylcarbene with trimethylenesulfide is directly observed by laser flash photolytic techniques.
A mild and chemoselective CALB biocatalysed synthesis of sulfoxides exploiting the dual role of AcOEt as solvent and reagent
Anselmi, Silvia,Liu, Siyu,Kim, Seong-Heun,Barry, Sarah M.,Moody, Thomas S.,Castagnolo, Daniele
supporting information, p. 156 - 161 (2021/01/14)
A mild, chemoselective and sustainable biocatalysed synthesis of sulfoxides has been developed exploiting CALB and using AcOEt with a dual role of more environmentally friendly reaction solvent and enzyme substrate. A series of sulfoxides, including the drug omeprazole, have been synthesised in high yields and with excellent E-factors.
Ruthenium-catalyzed decarboxylative C-S cross-coupling of carbonothioate: synthesis of allyl(aryl)sulfide
Zheng, Ren-Hua,Guo, Hai-Chang,Chen, Ting-Ting,Huang, Qing,Huang, Guo-Bo,Jiang, Hua-Jiang
, p. 25123 - 25126 (2018/07/29)
A novel ruthenium-catalyzed decarboxylative cross-coupling of carbonothioate is disclosed. This method provides straightforward access to the corresponding allyl(aryl)sulfide derivatives in generally good to excellent yields under mild conditions and feat
