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2H-1-Benzopyran-2-one, 6-amino-3-(4-aminophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

189310-22-3

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189310-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189310-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,3,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 189310-22:
(8*1)+(7*8)+(6*9)+(5*3)+(4*1)+(3*0)+(2*2)+(1*2)=143
143 % 10 = 3
So 189310-22-3 is a valid CAS Registry Number.

189310-22-3SDS

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 6-amino-3-p-aminophenylchromen-2-one

1.2 Other means of identification

Product number -
Other names 6-Amino-3-(4-amino-phenyl)-chromen-2-one

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:189310-22-3 SDS

189310-22-3Relevant articles and documents

Fluorescent labeling of specific protein targets in vitro and in vivo

-

, (2008/06/13)

New methods are provided for the post-genomic era that will permit the analysis of the dynamic expression and localization of gene products in living cells. Herein we propose the development of such a method from a bioorganic approach involving organic sy

Synthesis and characterization of dimaleimide fluorogens designed for specific labeling of proteins

Girouard, Stephane,Houle, Marie-Helene,Grandbois, Alain,Keillor, Jeffrey W.,Michnick, Stephen W.

, p. 559 - 566 (2007/10/03)

A series of aromatic compounds were prepared bearing two maleimide groups attached directly to the fluorescent cores. The resulting derivatives do not fluoresce until the maleimide groups undergo their typical thiol addition reaction, thus removing their

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