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92906-36-0

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92906-36-0 Usage

General Description

7-HYDROXY-4-(4-PYRIDYL)COUMARIN is a chemical compound that belongs to the coumarin family. It is a derivative of coumarin, which is a naturally occurring compound found in many plants. This particular compound has a hydroxy group and a pyridyl group attached to the parent coumarin structure. It is commonly used as a fluorescent probe in biochemical and medical research, particularly for detecting and measuring oxidative stress and reactive oxygen species in cells and tissues. Additionally, it has been studied for its potential pharmacological properties, including anti-inflammatory and anticancer effects. Its unique structure and properties make it a valuable tool for studying biological processes and developing new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 92906-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,0 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92906-36:
(7*9)+(6*2)+(5*9)+(4*0)+(3*6)+(2*3)+(1*6)=150
150 % 10 = 0
So 92906-36-0 is a valid CAS Registry Number.

92906-36-0SDS

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 7-hydroxy-4-pyridin-4-ylchromen-2-one

1.2 Other means of identification

Product number -
Other names 7-Hydroxy-4-(4-pyridyl)coumarin

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:92906-36-0 SDS

92906-36-0Downstream Products

92906-36-0Relevant articles and documents

Design, synthesis, and 3D QSAR of novel potent and selective aromatase inhibitors

Leonetti, Francesco,Favia, Angelo,Rao, Angela,Aliano, Rosaria,Paluszcak, Anja,Hartmann, Rolf W.,Carotti, Angelo

, p. 6792 - 6803 (2007/10/03)

The design, synthesis, and biological evaluation of a series of new aromatase inhibitors bearing an imidazole or triazole ring linked to a fluorene (A), indenodiazine (B), or coumarin scaffold (C) are reported. Properly substituted coumarin derivatives di

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