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

35976-82-0

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35976-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35976-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35976-82:
(7*3)+(6*5)+(5*9)+(4*7)+(3*6)+(2*8)+(1*2)=160
160 % 10 = 0
So 35976-82-0 is a valid CAS Registry Number.

35976-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-butenyl sulfide

1.2 Other means of identification

Product number -
Other names 1-ethylthio-2-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:35976-82-0 SDS

35976-82-0Downstream Products

35976-82-0Relevant academic research and scientific papers

The Stabilization due to the Methyl Group in RSCH2CH=CHCH3

Kimmelma, Reijo

, p. 344 - 347 (2007/10/02)

Equilibrium constants for the isomerization reactions have been measured and the energy differences of the isomers have been calculated.According to these results a methyl group stabilizes the double bond by 12.8(5) kJ mol-1 and the RSCH2CH3 cis interaction is 3.7(4) kJ mol-1.

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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