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3-(7-Hydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-propionic acid, also known as 3-(7-hydroxy-4-methylcoumarin-3-yl)-propionic acid, is a chemical compound derived from the coumarin family. It features a 2-oxo-2H-chromene core structure with a hydroxyl group at the 7-position, a methyl group at the 4-position, and a propionic acid side chain attached at the 3-position. 3-(7-HYDROXY-4-METHYL-2-OXO-2H-CHROMEN-3-YL)-PROPIONIC ACID is known for its potential applications in various fields, including pharmaceuticals and as a building block for the synthesis of other organic compounds. Its chemical structure endows it with unique properties that can be exploited in the development of new drugs or chemical entities.

5852-06-2

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5852-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5852-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5852-06:
(6*5)+(5*8)+(4*5)+(3*2)+(2*0)+(1*6)=102
102 % 10 = 2
So 5852-06-2 is a valid CAS Registry Number.

5852-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(7-hydroxy-4-methyl-2-oxochromen-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-(7-Hydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-propionsaeure

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

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More Details:5852-06-2 SDS

5852-06-2Relevant academic research and scientific papers

Syntheses on the basis of 2H-chromen-2-one and 2H-chromene-2-thione

Avetisyan,Alvandzhyan

, p. 1063 - 1067 (2006)

4-Hydroxy-2H-chromen-2-one and 4-hydroxy-2H-chromene-2-thione reacted with allyl bromide, 1,1,3-trichloroprop-1-ene, and 1,3-dichlorobut-2-ene to give the corresponding ethers, which were oxidized to (2-oxo-2H-chromen-4-yloxy)acetic acid with potassium permanganate, and various derivatives of that acid were obtained. 3-(3,3-Dichloroprop-2-enyl)-7-hydroxy-4-methyl-2H-chromen-2-one and 3-(3,3-dichloroprop-2-enyl)-7-hydroxy-4-methyl-2H-chromene-2-thione were synthesized, and some their transformations were studied. Pleiades Publishing, Inc., 2006.

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