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(8-acetyloxy-2-oxo-4-phenylchromen-7-yl) acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24258-37-5

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24258-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24258-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24258-37:
(7*2)+(6*4)+(5*2)+(4*5)+(3*8)+(2*3)+(1*7)=105
105 % 10 = 5
So 24258-37-5 is a valid CAS Registry Number.

24258-37-5SDS

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 7,8-diacetoxy-4-phenylcoumarin

1.2 Other means of identification

Product number -
Other names 7,8-Diacetoxy-4-phenyl-cumarin

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:24258-37-5 SDS

24258-37-5Relevant academic research and scientific papers

An efficient ZrCl4 catalyzed one-pot solvent free protocol for the synthesis of 4-substituted coumarins

Sharma,Janardhan Reddy,Sree Lakshmi,Radha Krishna

, p. 6119 - 6121 (2007/10/03)

A versatile and efficient route to 4-substituted coumarins via a Pechmann reaction using ZrCl4 as the catalyst (10 mol %) is described. This method provides several advantages over alternative procedures such as mild, solvent-free conditions at ambient temperature, and direct isolation of the products in high yields.

Mechanism of biochemical action of substituted 4-methylcoumarins. Part 11: Comparison of the specificities of acetoxy derivatives of 4-methylcoumarin and 4-phenylcoumarin to acetoxycoumarins: Protein transacetylase

Kumar, Ajit,Singh, Brajendra K.,Tyagi, Rahul,Jain, Sapan K.,Sharma, Sunil K.,Prasad, Ashok K.,Raj, Hanumantharao G.,Rastogi, Ramesh C.,Watterson, Arthur C.,Parmar, Virinder S.

, p. 4300 - 4305 (2007/10/03)

Our earlier observations led to the identification of a microsomal enzyme termed as acetoxy drug: protein transacetylase (TAase) catalyzing the transfer of acetyl groups from acetylated polyphenols to the receptor proteins. TAase was conveniently assayed

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