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108679-56-7

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108679-56-7 Usage

General Description

2H-1-Benzopyran-2-one, 3,4-dihydro-4-(4-Methylphenyl)-, also known as 4-Methylumbelliferone, is a synthetic compound that belongs to the class of benzopyranones. It is commonly used in research and laboratory settings as a fluorescent dye and as a choleretic agent to increase bile flow. Additionally, it has been studied for its potential anti-inflammatory, anti-cancer, and anti-viral properties. Its chemical structure and properties make it an important tool in studying various biological processes and as a potential therapeutic agent in the treatment of certain diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 108679-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,7 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108679-56:
(8*1)+(7*0)+(6*8)+(5*6)+(4*7)+(3*9)+(2*5)+(1*6)=157
157 % 10 = 7
So 108679-56-7 is a valid CAS Registry Number.

108679-56-7SDS

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 3,4-dihydro-4-p-tolylcoumarin

1.2 Other means of identification

Product number -
Other names 3,4-DIHYDRO-4-(4-METHYLPHENYL)-2H-1-BENZOPYRAN-2-ONE

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:108679-56-7 SDS

108679-56-7Downstream Products

108679-56-7Relevant articles and documents

Organic Br?nsted acid-catalyzed cycloadditions of o-quinone methides with 1, 3-dicarbonlys: Facile access to xanthenones and chromanones

Kokkuvayil Vasu, Radhakrishnan,Parameswaran, Sasikumar,Puthiyaparambath, Sharathna,Suresh Varma, Sanjay,Thoppe Sivakumar, Priyadarshini

, (2021)

The in-situ generation of o-quinone methides and their inverse-electron-demand Diels–Alder reaction in the presence of pentacarboxycyclopentadiene—an organic Br?nsted acid—has been reported. The synthesis of xanthenones and chromanones in good to excellen

Single-step synthesis of 4-phenyl and 3,4-dihydro-4-phenyl coumarins using a recyclable Preyssler heteropolyacid catalyst under solvent-free reaction conditions

Escobar, Anglica M.,Ruiz, Diego M.,Autino, Juan C.,Romanelli, Gustavo P.

, p. 10109 - 10123 (2016/01/12)

4-Phenyl and 3,4-dihydro-4-phenylcoumarins were prepared by direct esterification of phenols with phenylpropiolic and cinnamic acids, respectively, using a compound with Preyssler structure (H14P5NaW30O110) (PA)

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