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Benzene, (1-butenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50550-52-2

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50550-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50550-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50550-52:
(7*5)+(6*0)+(5*5)+(4*5)+(3*0)+(2*5)+(1*2)=92
92 % 10 = 2
So 50550-52-2 is a valid CAS Registry Number.

50550-52-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name but-1-enylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names 1-thiophenyl-1-butene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50550-52-2 SDS

50550-52-2Relevant academic research and scientific papers

The photochemical generation of α-sulfur-substituted cyclopropylcarbinyl radicals and their utilization as a mechanistic probe for electron transfer in the peroxide-sulfide reaction

Adam, Waldemar,Heil, Markus

, p. 1730 - 1736 (2007/10/02)

The photolytically induced n-Bu3SnH reduction of α-chloro-substituted sulfides 4 and photochemical addition of BrCCl3 to thiones 7 afford α-sulfur-substituted cyclopropylcarbinyl radicals, which rearrange efficiently to afford thioen

Application of Free Radical Substitution Reaction into Interconversion of 1-Alkenylsulfides, 1-Alkenylgermanes, and 1-Alkenylstannanes

Ichinose, Yoshifumi,Oshima, Koichiro,Utimoto, Kiitiro

, p. 669 - 672 (2007/10/02)

Treatment of 1-alkenylsulfides or 1-alkenylstannanes with Ph3GeH in the presence of Et3B provides 1-alkenyltriphenylgermanes in good yields. 1-Alkenylstannanes are converted into 1-alkenylsulfides easily with PhSH-Et3B, whereas 1-alkenyltriphenylgermanes are recovered unchanged upon treatment with Ph3SnH-Et3B or PhSH-Et3B.

PREPARATION OF 1-ALKENYL PHENYL SULFIDES BY THE NICKEL(II)-COMPLEXES CATALYZED COUPLING REACTION OF 3-METHOXY-1-PHENYLTHIO-1-PROPENE WITH GRIGNARD REAGENTS

Sugimura, Hideyuki,Takei, Hisashi

, p. 1505 - 1508 (2007/10/02)

The reaction of on 3-methoxy-1-phenylthio-1-propene with aryl and primary alkyl Grignard reagents in the presence of nickel(II)-phosphine complex in benzene or toluene proceeded chemo- and regioselectively to give 1-alkenyl phenyl sulfides in high yields.

Selective Condensation of titanium Reagent with Carbonyl Compounds

Furuta, Kyoji,Ikeda, Yoshihiko,Meguriya, Noriyuki,Ikeda, Nobuo,Yamamoto, Hisashi

, p. 2781 - 2790 (2007/10/02)

titanium reagent generated easily from allyl ethyl sulfides condensed with aldehydes to give erythro-β-hydroxy sulfides in highly regio- and stereoselective manner.In contrast, crotyl ethyl sulfide reacted with aldehydes affording δ-hydroxy vinyl sulfide exclusively.The substitution pattern of the starting sulfide can have a pronounced effect on the selectivity in this condensation reaction, erythro-β-Hydroxy sulfide obtained was transfromed stereoselectively to the trans-vinyloxirane or 1,3-alkadiene.

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