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1H-Pyrrole, 2,3-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

638-31-3

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638-31-3 Usage

Derivative of pyrrole

1H-Pyrrole, 2,3-dihydrois a chemical compound that is a derivative of pyrrole, a heterocyclic aromatic organic compound.

Physical properties

It is a colorless to light yellow liquid with a slightly ammonia-like odor.

Use in organic synthesis

The compound is commonly used as a building block in organic synthesis.

Applications in industries

It has applications in the pharmaceutical and chemical industries.

Synthesis of various compounds

1H-Pyrrole, 2,3-dihydrois known for its use in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds.

Important intermediate

It is an important intermediate in the production of various heterocyclic compounds.

Involvement in chemical reactions

1H-Pyrrole, 2,3-dihydrocan be found in a variety of chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 638-31-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 638-31:
(5*6)+(4*3)+(3*8)+(2*3)+(1*1)=73
73 % 10 = 3
So 638-31-3 is a valid CAS Registry Number.

638-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydropyrrole

1.2 Other means of identification

Product number -
Other names 2-pyrroline

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:638-31-3 SDS

638-31-3Relevant academic research and scientific papers

Asymmetric Ring Opening/Cyclization/Retro-Mannich Reaction of Cyclopropyl Ketones with Aryl 1,2-Diamines for the Synthesis of Benzimidazole Derivatives

Xia, Yong,Lin, Lili,Chang, Fenzhen,Liao, Yuting,Liu, Xiaohua,Feng, Xiaoming

, p. 12228 - 12232 (2016)

A highly efficient asymmetric ring-opening/cyclization/retro-Mannich reaction of cyclopropyl ketones with aryl 1,2-diamines has been realized using a chiral N,N′-dioxide/ScIIIcatalyst. Benzimidazoles containing chiral side chains were generated under mild reaction conditions in excellent outcomes (up to 99 % yield and 97 % ee). This method also provides efficient access to chiral benzimidazole-substituted amide and cycloheptene derivatives.

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