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2H-1-Benzopyran-6-carboxylic acid, 5-hydroxy-2,2-dimethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55932-36-0

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55932-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55932-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,3 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55932-36:
(7*5)+(6*5)+(5*9)+(4*3)+(3*2)+(2*3)+(1*6)=140
140 % 10 = 0
So 55932-36-0 is a valid CAS Registry Number.

55932-36-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-2,2-dimethyl-2H-chromene-6-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-carboxylate

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:55932-36-0 SDS

55932-36-0Relevant academic research and scientific papers

Synthesis of 3,4-dihydro-2H-benzopyrans from phenols and α,β-unsaturated carbonyl compounds

Saimoto, Hiroyuki,Ogo, Yoshie,Komoto, Mie,Morimoto, Minoru,Shigemasa, Yoshihiro

, p. 2051 - 2054 (2007/10/03)

The reaction between 2′,4′-dihydroxyacetophenone and methyl vinyl ketone catalyzed by CaCl2/KOH in aqueous methanol yielded a 1,4-adduct, which was cyclized to 3,4-dihydro-2H-benzopyran (4) by acidic treatment. Analogous reaction using α, β-unsaturated aldehydes afforded benzopyrans (4) or (5) in a one-pot reaction. This method was successfully applied to the synthesis of β-tubaic acid (6), an antimicrobial 2H-1-benzopyran-6-carboxylic acid.

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