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3-(2-Benzoxazolyl)umbelliferyl acetate is a synthetic chemical compound that serves as a fluorogenic substrate in enzymatic assays, specifically for the detection and measurement of glycosidase enzyme activity. Its unique structure, featuring a benzoxazole ring and an umbelliferyl group, allows it to emit fluorescence upon enzymatic hydrolysis, making it an invaluable tool in the study of enzyme kinetics and specificity.

97004-78-9

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97004-78-9 Usage

Uses

Used in Biochemistry Research:
3-(2-Benzoxazolyl)umbelliferyl acetate is used as a substrate in enzymatic assays for the detection and measurement of glycosidase enzyme activity. Its fluorogenic properties enable researchers to monitor the activity of these enzymes through the emitted fluorescence, providing insights into enzyme kinetics and specificity.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-(2-Benzoxazolyl)umbelliferyl acetate is utilized for the study of enzyme kinetics and inhibitor screening. Its ability to fluoresce upon enzymatic hydrolysis aids in the identification and development of potential enzyme inhibitors, which can be crucial in the discovery of new drugs targeting specific glycosidase enzymes.

Check Digit Verification of cas no

The CAS Registry Mumber 97004-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97004-78:
(7*9)+(6*7)+(5*0)+(4*0)+(3*4)+(2*7)+(1*8)=139
139 % 10 = 9
So 97004-78-9 is a valid CAS Registry Number.

97004-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(1,3-benzoxazol-2-yl)-2-oxochromen-7-yl] acetate

1.2 Other means of identification

Product number -
Other names 7-acetoxy-3-(2-benzoxazolyl)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:97004-78-9 SDS

97004-78-9Downstream Products

97004-78-9Relevant academic research and scientific papers

Synthesis of Some Coumarin Derivatives as Potential Laser Dyes

Elnagdi, M. H.,Abdallah, S. O.,Ghoneim, K. M.,Ebied, E. M.,Kassab, K. N.

, p. 375 - 384 (2007/10/03)

With a view to extend the tunability range and maximum output of the coumarin series of dyes, fifteen new 3-substituted 7-hydroxycoumarins emitting in the blue-green region of the visible spectrum are synthesized, and some of them showed laser activity.

Syntheses and Spectral Properties of Longwave Absorbing and Fluorescing Substrates for the Direct and Continuous Kinetic Assay of Carboxylesterases, Phosphatases, and Sulfatases

Koller, Ernst,Wolfbeis, Otto S.

, p. 65 - 76 (2007/10/02)

Syntheses, absorption and fluorescence properties for a series of new enzyme substrates are described, which are derived from 7-hydroxycoumarins possessing electron-withdrawing substituents in position 3.The new substrates are advantageous over existing ones in that they exhibit longwave absorption and fluorescence maxima as well as large Stokes' shifts.In addition, their pKa values, which are usually between 6.0 and 7.0, allow the direct and continuous kinetic assay of hydrolases such as esterases, phosphatases, and sulfatases. - Keywords: Enzyme substrates; Absorption spectra; Fluorescence spectra

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