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Ethanethioamide, N-[2-(3,4-dimethoxyphenyl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91564-56-6

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91564-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91564-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,6 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91564-56:
(7*9)+(6*1)+(5*5)+(4*6)+(3*4)+(2*5)+(1*6)=146
146 % 10 = 6
So 91564-56-6 is a valid CAS Registry Number.

91564-56-6SDS

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 N-[2-(3,4-dimethoxyphenyl)ethyl]ethanethioamide

1.2 Other means of identification

Product number -
Other names Ethanethioamide,N-[2-(3,4-dimethoxyphenyl)ethyl]

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:91564-56-6 SDS

91564-56-6Downstream Products

91564-56-6Relevant academic research and scientific papers

Synthesis and spectroscopic studies of some hydrogenated thiazolo[2,3-a]isoquinolines

Rozwadowska, Maria D,Sulima, Agnieszka

, p. 3499 - 3506 (2001)

Dihydro-5H-thiazolo[2,3-a]isoquinolinones (1-6) and tetrahydro-5H-thiazolo[2,3a]isoquinolines (7-12) have been prepared from 3,4-dihydroisoquinoline derivatives under the action of α-mercapto alkanoic acids or ethylene sulfide, respectively. In the synthe

Application of the ortho-Lithiation-Cyclization Strategy to N-Benzyl- and N-Phenethylamine Derivatives

Lete, Esther,Collado, M. Isabel,Sotomayor, Nuria,Vicente, Teresa,Villa, Maria-Jesus

, p. 1751 - 1758 (2007/10/03)

The ortho-lithiation-cyclization of iodinated N,N-diacylphenethylamines provides a convenient method for the preparation of 2-(2-acetoamidoethyl)acetophenones and 2-(2-benzamidoethyl)benzophenones, which could be easily transformed into dihydroisoquinolines.By contrast, the N-ethylamino, N-acetylamino, and N-trimethylsilylamino moieties studied as ortho-directing groups provide poor assistance to the metalation of N-benzyl- and N-phenyethylamines and the corresponding isoindolone or isoquinolone derivatives are obtained in low yields.

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