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1197-13-3

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1197-13-3 Usage

Uses

Methyl 5-formylpyrrole-2-carboxylate

Check Digit Verification of cas no

The CAS Registry Mumber 1197-13-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1197-13:
(6*1)+(5*1)+(4*9)+(3*7)+(2*1)+(1*3)=73
73 % 10 = 3
So 1197-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO3/c1-11-7(10)6-3-2-5(4-9)8-6/h2-4,8H,1H3

1197-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-formyl-1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Formylpyrrole-2-carboxylic acid methyl ester

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:1197-13-3 SDS

1197-13-3Relevant articles and documents

Synthesis and characterization of Boc-protected 4-amino- and 5-amino-pyrrole-2-carboxylic acid methyl esters

Chakraborty, Tushar Kanti,Udawant, Sandip P.,Roy, Saumya,Mohan, Bajjuri Krishna,Rao, Kolla Srinivasa,Dutta, Samit Kumar,Kunwar, Ajit Chand

, p. 4631 - 4634 (2006)

Syntheses of Boc-protected 4-amino- and 5-amino-pyrrole-2-carboxylic acid methyl esters have been achieved and the structures of these compounds have been fully characterized by detailed NMR studies.

Discovery of a novel HCV helicase inhibitor by a de novo drug design approach

Kandil, Sahar,Biondaro, Sonia,Vlachakis, Dimitrios,Cummins, Anna-Claire,Coluccia, Antonio,Berry, Colin,Leyssen, Pieter,Neyts, Johan,Brancale, Andrea

, p. 2935 - 2937 (2009)

Herein we report a successful application of a computer-aided design approach to identify a novel HCV helicase inhibitor. A de novo drug design methodology was used to generate an initial set of structures that could potentially bind to a putative binding

The role of N-terminal heterocycles in hydrogen bonding to α-chymotrypsin

Schumann, Nicholas C.,Bruning, John,Marshall, Andrew C.,Abell, Andrew D.

, p. 396 - 399 (2019)

A series of dipeptide aldehydes containing different N-terminal heterocycles was prepared and assayed in vitro against α-chymotrypsin to ascertain the importance of the heterocycle in maintaining a β-strand geometry while also providing a hydrogen bond do

Design, Sustainable Synthesis, and Programmed Reactions of Templated N-Heteroaryl-Fused Vinyl Sultams

Laha, Joydev K.,Sharma, Shubhra,Kirar, Seema,Banerjee, Uttam C.

, p. 9350 - 9359 (2017/09/23)

A de novo design and synthesis of N-heteroaryl-fused vinyl sultams as templates for programming chemical reactions on vinyl sultam periphery or (hetero)aryl ring is described. The key features include rational designing and sustainable synthesis of the template, customized reactions of vinyl sultams at C=C bond or involving N-S bond cleavage, and reactions on the periphery of the heteroaryl ring for late-stage diversification. The simple, easy access to the template coupled with opportunities for the synthesis of diversely functionalized heterocyles from a single template constitutes a rare study in contemporary organic synthesis.

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