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Benzene, 1,1'-[(1-butyl-1,2-ethenediyl)bis(thio)]bis-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120915-22-2

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120915-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120915-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,1 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120915-22:
(8*1)+(7*2)+(6*0)+(5*9)+(4*1)+(3*5)+(2*2)+(1*2)=92
92 % 10 = 2
So 120915-22-2 is a valid CAS Registry Number.

120915-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1,2-bis(phenylthio)-1-hexene

1.2 Other means of identification

Product number -
Other names 1,2-bis(phenylthio)hex-1-ene

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:120915-22-2 SDS

120915-22-2Downstream Products

120915-22-2Relevant academic research and scientific papers

Convenient method for the addition of disulfides to alkenes

Yamagiwa, Noriyuki,Suto, Yutaka,Torisawa, Yasuhiro

, p. 6197 - 6201 (2008/03/14)

Catalytic disulfenylation reaction of alkenes by common Lewis acids has been investigated in detail. While reactions by FeCl3 were feasible with cycloalkenes and other simple alkenes, much faster and excellent conversions were possible by AlCl

Disulfidation of Alkynes and Alkenes with Gallium Trichloride

Usugi, Shin-Ichi,Yorimitsu, Hideki,Shinokubo, Hiroshi,Oshima, Koichiro

, p. 601 - 603 (2007/10/03)

(Matrix presented) Treatment of diphenyl disulfide and terminal alkynes with gallium trichloride afforded (E)-1,2-diphenylthio-1-alkenes selectively (E/Z > 20/1). Alkenes also underwent this reaction to form trans adducts.

Boron Trifluoride-promoted Reaction of 4'-Nitrobenzenesulphenanilide with Alkynes. Formal Addition of Benzenesulphenyl Fluoride to Carbon-Carbon Triple Bonds

Benati, Luisa,Montevecchi, P. Carlo,Spagnolo, Piero

, p. 1690 - 1695 (2007/10/02)

The BF3-promoted reaction of 4'-nitrobenzenesulphenanilide with simple alkyl- and aryl-alkynes at 80 deg C in the presence of tetrabutylammonium tetrafluoroborate provides a one-pot synthetic route to β-fluorovinyl sulphides via a formal regioselective and trans-stereospecific addition of benzenesulphenyl fluoride towards carbon-carbon triple bonds.

Free Radical Addition of Thiophenol to 3-Substituted 1-Alkyne with or without Migration of the Substituents

Miyake, Hideyoshi,Yamamura, Kimiaki

, p. 3752 - 3754 (2007/10/02)

Thiophenol reacts with 3-phenylthio- and 3-bromo-1-alkyne in the presence of radical initiator to give 1,2-bis(phenylthio)-1-alkene and 2-bromo-1-phenylthio-1-alkene.

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