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5527-91-3

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  • 4H-1-Benzopyran-2-carboxylicacid, 6-ethyl-4-oxo-

    Cas No: 5527-91-3

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5527-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5527-91-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5527-91:
(6*5)+(5*5)+(4*2)+(3*7)+(2*9)+(1*1)=103
103 % 10 = 3
So 5527-91-3 is a valid CAS Registry Number.

5527-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethyl-4-oxochromene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-ethylchromone-2-carboxylic acid

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:5527-91-3 SDS

5527-91-3Relevant articles and documents

Chromene-containing aromatic sulfonamides with carbonic anhydrase inhibitory properties

Angeli, Andrea,Kartsev, Victor,Petrou, Anthi,Pinteala, Mariana,Brovarets, Volodymyr,Slyvchuk, Sergii,Pilyo, Stepan,Geronikaki, Athina,Supuran, Claudiu T.

, (2021/05/19)

Carbonic anhydrases (CAs, EC 4.2.1.1) catalyze the essential reaction of CO2 hydration in all living organisms, being actively involved in the regulation of a plethora of patho/physiological conditions. A series of chromene-based sulfonamides were synthesized and tested as possible CA inhibitors. Their inhibitory activity was assessed against the cytosolic human isoforms hCA I, hCA II and the transmembrane hCA IX and XII. Several of the investigated derivatives showed interesting inhibition activity towards the tumor associate isoforms hCA IX and hCA XII. Furthermore, computational procedures were used to investigate the binding mode of this class of compounds, within the active site of hCA IX.

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