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phenyl 2-oxo-2H-chromene-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53992-24-8

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53992-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53992-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,9 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53992-24:
(7*5)+(6*3)+(5*9)+(4*9)+(3*2)+(2*2)+(1*4)=148
148 % 10 = 8
So 53992-24-8 is a valid CAS Registry Number.

53992-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl 2-oxochromene-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Carbophenoxycumarin

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:53992-24-8 SDS

53992-24-8Relevant academic research and scientific papers

METHODS OF IDENTIFYING CROSSLINKING MOLECULES FOR POLYMERS

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Paragraph 0093; 0094, (2015/06/03)

Methods for screening molecules or moieties for their ability to crosslink are disclosed. An aromatic carbonate, aromatic ester, or aliphatic ester group is attached to the molecule to mimic the presence of a polymer. A solution of the modified molecule i

Coumarinic derivatives as mechanism-based inhibitors of α-chymotrypsin and human leukocyte elastase

Pochet, Lionel,Doucet, Caroline,Dive, Georges,Wouters, Johan,Masereel, Bernard,Reboud-Ravaux, Michele,Pirotte, Bernard

, p. 1489 - 1501 (2007/10/03)

Novel coumarinic derivatives were synthesized and tested for their inhibitory potency toward α-CT and HLE. Cycloalkyl esters and amides were found to be essentially inactive on both enzymes. On the opposite, aromatic esters strongly inactivated α-CT where

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