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5399-21-3

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5399-21-3 Usage

General Description

2-Methyl-5,6-dihydro-4H-pyran-3-carboxylic acid is a compound that belongs to the class of pyran carboxylic acids. It is a derivative of pyran, a six-membered heterocyclic ring containing oxygen. This chemical has a molecular formula of C7H10O3 and a molecular weight of 142.15 g/mol. It is used in the pharmaceutical and chemical industries for the synthesis of various organic compounds and as a building block in the production of drugs. 2-METHYL-5,6-DIHYDRO-4H-PYRAN-3-CARBOXYLIC ACID has also been studied for its potential biological activities and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5399-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5399-21:
(6*5)+(5*3)+(4*9)+(3*9)+(2*2)+(1*1)=113
113 % 10 = 3
So 5399-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O3/c1-5-6(7(8)9)3-2-4-10-5/h2-4H2,1H3,(H,8,9)

5399-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Methyl-3,4-dihydro-2H-pyran-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3,4-Dihydro-6-methyl-2H-pyran-5-carboxylic acid

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:5399-21-3 SDS

5399-21-3Relevant articles and documents

Catalytic enantioselective nazarov cyclization: Construction of vicinal all-carbon-atom quaternary stereocenters

Jolit, Anais,Walleser, Patrick M.,Yap, Glenn P. A.,Tius, Marcus A.

supporting information, p. 6180 - 6183 (2014/06/23)

The diastereoselective asymmetric synthesis of vicinal all-carbon-atom quaternary stereocenters is a challenging problem in organic synthesis for which only few solutions have been described. A catalytic asymmetric Nazarov cyclization of fully substituted dienones that provides cyclopentenone derivatives with vicinal quaternary stereocenters in high optical purity and as single diastereoisomers is now reported.

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