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Pyridine, 2-[2-[(phenylmethyl)thio]ethenyl]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94191-09-0

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94191-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94191-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,9 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94191-09:
(7*9)+(6*4)+(5*1)+(4*9)+(3*1)+(2*0)+(1*9)=140
140 % 10 = 0
So 94191-09-0 is a valid CAS Registry Number.

94191-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis benzyl 2-(2-pyridyl)vinyl sulfide

1.2 Other means of identification

Product number -
Other names 2-((Z)-2-Benzylsulfanyl-vinyl)-pyridine

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:94191-09-0 SDS

94191-09-0Downstream Products

94191-09-0Relevant academic research and scientific papers

Anti-Markovnikov stereoselective hydroamination and hydrothiolation of (hetero)aromatic alkynes using a metal-free cyclic trimeric phosphazene base

Zhao, Na,Lin, Chengdong,Wen, Lirong,Li, Zhibo

, p. 3432 - 3440 (2019/05/15)

Hydroamination and hydrothiolation are the most efficient and completely atom-economical process to construct important enamine and vinyl sulfide intermediates in pharmaceutical and organic chemistry. The cyclic trimeric phosphazene base (CTPB) showed gre

Chemistry of Thienopyridines. XXXI. A New Synthesis of Thienopyridine and Studies on Direct Substitution into Its Thiophene Ring

Klemm, L. H.,Louris, John N.

, p. 785 - 790 (2007/10/02)

Thienopyridine (1) is synthesized in 65percent overall yield for two steps which consist of addition of toluene-α-thiol to 2-ethynylpyridine plus vacuum pyrolysis of the addend (7).Cis and trans forms of 7 are described.Compound 1 undergoes (a) ele

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