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1H-Pyrrole-3-carboxylic acid, 1,2-dimethyl-4-(phenylthio)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112799-34-5

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112799-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112799-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,9 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112799-34:
(8*1)+(7*1)+(6*2)+(5*7)+(4*9)+(3*9)+(2*3)+(1*4)=135
135 % 10 = 5
So 112799-34-5 is a valid CAS Registry Number.

112799-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Dimethyl-4-phenylthiopyrrol-3-carbonsaeuremethylester

1.2 Other means of identification

Product number -
Other names -

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:112799-34-5 SDS

112799-34-5Relevant academic research and scientific papers

4-(Phenylthio)-pyrrole-3-carboxylic Acid Esters

Eiden, Fritz,Grusdt, Ulrike

, p. 1020 - 1031 (2007/10/02)

Dihydro(dimethoxy)methylfurancarboxylic acid esters 4A/4B have been applied to the synthesis of the title compounds.With amines as catalysts they react with thiophenols to give the addition products 12a-d, which upon heating with acids eliminate methanol to form the furancarboxylic acid esters 13a-b and 17, whereas reactions with ammonia or amines lead to the pyrrolecarboxylic acid esters 20a-e.Reactions of 4 with 2-aminothiophenol yield the fused pyrrole and pyrrolidine derivatives 15 and 16.Compounds 20b and e were transformed to the benzothiopyranopyrrole carboxylic acid esters 23a and b.

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