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2H-1-Benzopyran-2-one, 4-[3-(acetyloxy)-4-methoxyphenyl]-5,7-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88126-49-2

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88126-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88126-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,2 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88126-49:
(7*8)+(6*8)+(5*1)+(4*2)+(3*6)+(2*4)+(1*9)=152
152 % 10 = 2
So 88126-49-2 is a valid CAS Registry Number.

88126-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3'-acetoxy-4'-methoxyphenyl)-5,7-dimethoxycoumarin

1.2 Other means of identification

Product number -
Other names Acetic acid 5-(5,7-dimethoxy-2-oxo-2H-chromen-4-yl)-2-methoxy-phenyl ester

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:88126-49-2 SDS

88126-49-2Relevant academic research and scientific papers

Synthesis and antiprotozoal activity of 4-arylcoumarins

Pierson, Jean-Thomas,Dumètre, Aurélien,Hutter, Sébastien,Delmas, Florence,Laget, Michèle,Finet, Jean-Pierre,Azas, Nadine,Combes, Sébastien

scheme or table, p. 864 - 869 (2010/04/26)

A large series of 4-arylcoumarins was synthesized by Suzuki-Miyaura cross-coupling reaction and evaluated for antiprotozoal activity against Plasmodium falciparum and Leishmania donovani. Several compounds were found to strongly inhibit the proliferation

Short synthesis of cytotoxic 4-arylcoumarins

Rizzi, Eleonora,Dallavalle, Sabrina,Merlini, Lucio,Pratesi, Graziella,Zunino, Franco

, p. 1117 - 1122 (2007/10/03)

A short synthesis of cytotoxic 4-arylcoumarins via condensation of phenols with cinnamic acids in the presence of CF3COOH, followed by dehydrogenation with DDQ, is described. Copyright Taylor & Francis Group, LLC.

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