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1H-Pyrrole-2-carboxylicacid,2-hydroxyethylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

668987-22-2

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668987-22-2 Usage

Chemical structure

A pyrrole ring with a carboxylic acid group and a hydroxyethyl group attached

Usage in pharmaceutical industry

As an intermediate for the synthesis of various drugs and pharmaceuticals

Application in organic synthesis

As a building block to create other compounds with specific properties

Potential applications

Research and development in fields such as medicine and material science

Check Digit Verification of cas no

The CAS Registry Mumber 668987-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,8,9,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 668987-22:
(8*6)+(7*6)+(6*8)+(5*9)+(4*8)+(3*7)+(2*2)+(1*2)=242
242 % 10 = 2
So 668987-22-2 is a valid CAS Registry Number.

668987-22-2SDS

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 2-hydroxyethyl 1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-PYRROLE-2-CARBOXYLIC ACID,2-HYDROXYETHYL 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:668987-22-2 SDS

668987-22-2Downstream Products

668987-22-2Relevant academic research and scientific papers

Synthesis and Conformational Properties of 3,4-Difluoro- l -prolines

Hofman, Gert-Jan,Ottoy, Emile,Light, Mark E.,Kieffer, Bruno,Martins, Jose C.,Kuprov, Ilya,Sinnaeve, Davy,Linclau, Bruno

, p. 3100 - 3120 (2019)

Fluorinated proline derivatives have found diverse applications in areas ranging from medicinal chemistry over structural biochemistry to organocatalysis. Depending on the stereochemistry of monofluorination at the proline 3- or 4-position, different effe

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