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92424-80-1

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92424-80-1 Usage

Chemical Structure

Chromen-4-one core with hydroxyl, nitro, and phenyl substituents

Derivative of

Coumarin

Pharmacological Properties

Antioxidant, anti-inflammatory, anticancer activities

Therapeutic Applications

Potential treatment for cancer and inflammation-related disorders

Research Focus

Potential use in drug development and medicinal compounds

Interest for Investigation

Unique chemical structure and biological activities make it an interesting target for further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 92424-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,2 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92424-80:
(7*9)+(6*2)+(5*4)+(4*2)+(3*4)+(2*8)+(1*0)=131
131 % 10 = 1
So 92424-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H9NO5/c17-11-8-13(9-4-2-1-3-5-9)21-12-7-6-10(16(19)20)15(18)14(11)12/h1-8,18H

92424-80-1SDS

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 5-hydroxy-6-nitro-2-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 6-Nitro-5-hydroxy-flavon

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:92424-80-1 SDS

92424-80-1Relevant articles and documents

α-Glucosidase inhibition of 6-hydroxyflavones. Part 3: Synthesis and evaluation of 2,3,4-trihydroxybenzoyl-containing flavonoid analogs and 6-aminoflavones as α-glucosidase inhibitors

Gao, Hong,Kawabata, Jun

, p. 1661 - 1671 (2007/10/03)

The SAR studies suggested that the C-ring of baicalein (1) was not necessary for the activity, and validated the importance of 2,3,4- trihydroxybenzoyl structure of 1. Thus, a series of 2,3,4-trihydroxybenzoyl- containing flavonoid analogs were investigat

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