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144223-32-5

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144223-32-5 Usage

Family

Benzotriazoles and Pyrroles

Function

UV absorber and stabilizer

Applications

Sunscreens
Coatings
Plastics
Artwork preservation
Protection of polymers and materials from UV radiation

Ability

Absorbs and dissipates UV radiation

Purpose

Protects materials from degradation caused by sunlight exposure

Check Digit Verification of cas no

The CAS Registry Mumber 144223-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,2 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144223-32:
(8*1)+(7*4)+(6*4)+(5*2)+(4*2)+(3*3)+(2*3)+(1*2)=95
95 % 10 = 5
So 144223-32-5 is a valid CAS Registry Number.

144223-32-5 Well-known Company Product Price

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  • Aldrich

  • (631892)  1-(2-Pyrrolecarbonyl)benzotriazole  97%

  • 144223-32-5

  • 631892-1G

  • 972.27CNY

  • Detail

144223-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzotriazol-1-yl(1H-pyrrol-2-yl)methanone

1.2 Other means of identification

Product number -
Other names 1-(2-pyrrolecarbonyl)-benzotriazole

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:144223-32-5 SDS

144223-32-5Relevant articles and documents

Regiospecific C-acylation of pyrroles and indoles using N-acylbenzotriazoles

Katritzky, Alan R.,Suzuki, Kazuyuki,Singh, Sandeep K.,He, Hai-Ying

, p. 5720 - 5723 (2007/10/03)

Reactions of pyrrole (2) or 1-methylpyrrole (4) with readily available N-acylbenzotriazoles 1a - g (RCOBt, where R = 4-tolyl, 4-nitrophenyl, 4-diethylaminophenyl, 2-furyl, 2-pyridyl, 2-indolyl, or 2-pyrrolyl) in the presence of TiCl4 produced 2

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