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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.

92906-36-0

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92906-36-0 Usage

Uses

Used in Biochemical and Medical Research:
7-HYDROXY-4-(4-PYRIDYL)COUMARIN is used as a fluorescent probe for detecting and measuring oxidative stress and reactive oxygen species in cells and tissues. Its fluorescence properties allow for the monitoring of these processes, which are crucial for understanding various diseases and conditions.
Used in Pharmaceutical Research:
7-HYDROXY-4-(4-PYRIDYL)COUMARIN is studied for its potential pharmacological properties, including anti-inflammatory and anticancer effects. Its unique structure and properties make it a promising candidate for the development of new therapeutic agents.
Used in Drug Development:
Due to its potential pharmacological properties, 7-HYDROXY-4-(4-PYRIDYL)COUMARIN is used in the development of new drugs targeting various diseases and conditions. Its unique structure and properties can be leveraged to create novel therapeutic agents with improved efficacy and safety profiles.
Used in Diagnostics:
7-HYDROXY-4-(4-PYRIDYL)COUMARIN's fluorescent properties can be utilized in diagnostic applications, such as the detection of specific biomarkers or the assessment of cellular health. Its ability to measure oxidative stress and reactive oxygen species can aid in the diagnosis and monitoring of various diseases and conditions.
Used in Environmental Research:
7-HYDROXY-4-(4-PYRIDYL)COUMARIN can be employed in environmental research to study the effects of pollutants and other environmental factors on cells and tissues. Its ability to detect and measure oxidative stress and reactive oxygen species can provide valuable insights into the impact of environmental stressors on biological systems.

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 academic research and scientific papers

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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