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

123476-57-3

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123476-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123476-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,7 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123476-57:
(8*1)+(7*2)+(6*3)+(5*4)+(4*7)+(3*6)+(2*5)+(1*7)=123
123 % 10 = 3
So 123476-57-3 is a valid CAS Registry Number.

123476-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-benzylpyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-benzyl-1H-pyrrole-2-carboxylate

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:123476-57-3 SDS

123476-57-3Relevant academic research and scientific papers

Nouvelle methode de synthese de pyrroles sous micro-ondes

Oussaid, Boualem,Garrigues, Bernard,Soufiaoui, Mohammed

, p. 2483 - 2485 (2007/10/02)

The dehydrogenation of pyrrolidines by manganese dioxide, under microwave irradiation, provides a mild method for the preparation of substituted pyrroles.

Preparation of pyrroles by dehydrogenation of pyrrolidines with manganese dioxide

Bonnaud,Bigg

, p. 465 - 467 (2007/10/02)

The dehydrogenation of pyrrolidines by activated manganese dioxide provides a fairly general and mild method for the preparation of substituted pyrroles.

Pyrroles from 3-Alkoxyacroleins and CH-acidic α-Aminoacetic Acid Derivatives

Walizei, Gul Hassan,Breitmaier, Eberhard

, p. 337 - 340 (2007/10/02)

2-Alkoxycarbonylpyrroles and 2-cyanopyrroles 4 are prepared in a one-step synthesis by vinylogous amidation of 3-alkoxyacroleins 1 with glycine esters 2a-c and aminoacetonitrile (2d), followed by base-catalyzed cyclodehydration of the intermediate 3-aminoacroleins 3.The 3-hydroxypropyl function can be introduced into the pyrrole ring by using 3,4-dihydro-2H-pyran-5-carbaldehyde (5) as a cyclic 3-alkoxyacrolein.

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