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3-(p-nitrophenyl)-4,7-dihydroxycoumarin is a chemical compound characterized by its fluorogenic properties, which make it a valuable tool in the field of biochemistry and molecular biology. It is particularly known for its role as a substrate for the detection and measurement of enzyme activity, specifically β-glucuronidase. 3-(p-nitrophenyl)-4,7-dihydroxycoumarin's fluorescent nature allows for easy detection and quantification, facilitating the study of enzyme kinetics and substrate specificity in various biochemical processes.

67363-67-1

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67363-67-1 Usage

Uses

Used in Biochemical Research:
3-(p-nitrophenyl)-4,7-dihydroxycoumarin is used as a fluorogenic substrate for the detection of enzyme activity, particularly β-glucuronidase, in various biological samples. Its fluorescence upon enzymatic cleavage allows for the accurate measurement of enzyme activity, making it a useful tool for studying enzyme kinetics and substrate specificity.
Used in Molecular Biology:
In the field of molecular biology, 3-(p-nitrophenyl)-4,7-dihydroxycoumarin serves as a substrate for the measurement of β-glucuronidase activity, which is essential for understanding the mechanisms of enzyme action and their role in biological processes.
Used in Drug Discovery and Development:
3-(p-nitrophenyl)-4,7-dihydroxycoumarin has potential applications in drug discovery and development, particularly for screening enzyme inhibitors. Its ability to act as a substrate for β-glucuronidase makes it a valuable tool for identifying and evaluating potential inhibitors that can modulate enzyme activity, leading to the development of new therapeutic agents.
Used in Diagnostic Applications:
3-(p-nitrophenyl)-4,7-dihydroxycoumarin's fluorescent properties also make it suitable for diagnostic applications, where it can be used to detect and measure the presence of specific enzymes or enzyme activities in biological samples, aiding in the diagnosis of various diseases and conditions.
Used in Analytical Chemistry:
3-(p-nitrophenyl)-4,7-dihydroxycoumarin can be employed in analytical chemistry for the development of assays and methods to quantify enzyme activities, providing a sensitive and specific means of detecting and measuring enzymatic processes in various samples.

Check Digit Verification of cas no

The CAS Registry Mumber 67363-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,6 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67363-67:
(7*6)+(6*7)+(5*3)+(4*6)+(3*3)+(2*6)+(1*7)=151
151 % 10 = 1
So 67363-67-1 is a valid CAS Registry Number.

67363-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(p-nitrophenyl)-4,7-dihydroxycoumarin

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:67363-67-1 SDS

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