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21461-86-9

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21461-86-9 Usage

General Description

"(R)-2-Methyl-5-oxo-tetrahydrofurane-2-carboxylic acid" is a chemical compound with a molecular formula C7H10O4. It is a derivative of tetrahydrofuran and belongs to the class of carboxylic acids. (R)-2-Methyl-5-oxo-tetrahydrofurane-2-carboxylicacid exists in two enantiomeric forms, with the (R)-enantiomer being the more common form. It is used as a chiral starting material in organic synthesis and pharmaceutical research, as well as a building block for the synthesis of other organic compounds. The (R)-2-Methyl-5-oxo-tetrahydrofurane-2-carboxylic acid has potential applications in the development of new drugs, agrochemicals, and materials. It is important to handle this compound with care, as it may present hazards if not used or stored properly.

Check Digit Verification of cas no

The CAS Registry Mumber 21461-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,6 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21461-86:
(7*2)+(6*1)+(5*4)+(4*6)+(3*1)+(2*8)+(1*6)=89
89 % 10 = 9
So 21461-86-9 is a valid CAS Registry Number.

21461-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-Methyl-5-oxo-tetrahydrofurane-2-carboxylicacid

1.2 Other means of identification

Product number -
Other names (R)-tetrahydro-5-oxo-2-methyl-2-furancarboxylic 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:21461-86-9 SDS

21461-86-9Relevant articles and documents

Asymmetric synthesis of 2-alkyl-substituted 2-hydroxyglutaric acid γ-lactones

Paju, Anne,Laos, Marit,J?gi, Artur,P?ri, Malle,J??laid, Raissa,Pehk, T?nis,Kanger, T?nis,Lopp, Margus

, p. 4491 - 4493 (2007/10/03)

3-Alkyl-1,2-cyclopentanediones 1 are transformed into 2-alkyl-2-hydroxyglutaric acid γ-lactones 3 in up to 83% isolated yields and up to 96% ee, affording a simple access to many bioactive compounds, including diacylglycerol lactones (DAG-lactones).

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