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3-Furancarboxylic acid, 2,3-dihydro-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97222-13-4

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97222-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97222-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,2 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97222-13:
(7*9)+(6*7)+(5*2)+(4*2)+(3*2)+(2*1)+(1*3)=134
134 % 10 = 4
So 97222-13-4 is a valid CAS Registry Number.

97222-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2,3-dihydrofuran-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Furancarboxylic acid,2,3-dihydro-,phenylmethyl ester

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:97222-13-4 SDS

97222-13-4Relevant academic research and scientific papers

Synthesis of a Cyclobutanone Analogue of a β-Lactam Antibiotic

Lowe, Gordon,Swain, Steven

, p. 391 - 398 (2007/10/02)

A route has been developed which allows cyclobutanone analogues of β-lactam antibiotics to be synthesized and is illustrated by the synthesis of 6-oxo-7β-phenylacetamido-2-oxabicycloheptane-4α-carboxylic acid.Although this analogue (which contained some 7α-epimer) did not show significant antibacterial activity it was a weak inhibitor of Streptomyces R61 D,D-carboxypeptidase and a time-dependent inhibitor of E.coli R-TEM and B. cereus type I β-lactamases. 7β-Chloro-6-oxo-2-oxabicycloheptane-4α-carboxylic acid also exhibited time-dependent inhibition of these β-lactamases.

Synthesis of 7&β-Phenylacetamido-6-oxo-2-oxabicycloheptane-4&α-carboxylic acid, a Cyclobutanone Analogue of a &β-Lactam Antibiotic

Lowe, Gordon,Swain, Steven

, p. 1279 - 1281 (2007/10/02)

A route has been developed for the synthesis of cyclobutanone analogues of β-lactam antibiotics.

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