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2-Furancarboxylicacid,tetrahydro-2-methyl-4-methylene-5-oxo-,(2S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

314264-83-0

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314264-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 314264-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,2,6 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 314264-83:
(8*3)+(7*1)+(6*4)+(5*2)+(4*6)+(3*4)+(2*8)+(1*3)=120
120 % 10 = 0
So 314264-83-0 is a valid CAS Registry Number.

314264-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-2-methyl-4-methylene-tetrahydro-5-oxo-2-furancarboxylic acid

1.2 Other means of identification

Product number -
Other names (S)-2-Methyl-4-methylene-5-oxo-tetrahydro-furan-2-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:314264-83-0 SDS

314264-83-0Downstream Products

314264-83-0Relevant academic research and scientific papers

Enzymic resolution of an α-methylene-γ-lactonic ester

Pitacco, Giuliana,O Santi, Andrea Sessanta,Valentin, Ennio

, p. 3263 - 3267 (2000)

The possibility of using enzymes for the kinetic resolution of an α-methylene-γ-lactone was explored. The probe molecule, ethyl 2-methyl-4-methylene-tetrahydro-5-oxo-2-furancarboxylate was successfully resolved with Porcine pancreatic lipase and Candida rugosa lipase, in the presence of a cosolvent, leading to both enantiomers of the corresponding acid with high enantiomeric excesses. Copyright (C) 2000 Elsevier Science Ltd.

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