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2(3H)-Furanone, 4-(benzoyloxy)dihydro-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

207985-74-8

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207985-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207985-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,8 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 207985-74:
(8*2)+(7*0)+(6*7)+(5*9)+(4*8)+(3*5)+(2*7)+(1*4)=168
168 % 10 = 8
So 207985-74-8 is a valid CAS Registry Number.

207985-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3S)-5-oxooxolan-3-yl] benzoate

1.2 Other means of identification

Product number -
Other names 2(3H)-Furanone,4-(benzoyloxy)dihydro-,(4S)

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:207985-74-8 SDS

207985-74-8Relevant academic research and scientific papers

Organocatalytic asymmetric oxy-Michael addition to a γ-hydroxy- α,β-unsaturated thioester via hemiacetal intermediates

Okamura, Takaaki,Asano, Keisuke,Matsubara, Seijiro

supporting information; experimental part, p. 5076 - 5078 (2012/07/02)

We report an asymmetric oxy-Michael addition to a γ-hydroxy-α, β-unsaturated thioester via hemiacetal intermediates in the presence of Cinchona-alkaloid-thiourea-based bifunctional organocatalysts. This method provides a novel enantioselective route to β-hydroxy carboxyl compounds, which in turn can be used to synthesize valuable chiral building blocks.

METHOD FOR PREPARING (S)-3-HYDROXY-GAMMA-BUTYROLACTONE USING HYDROLASE

-

Page/Page column 6-7, (2008/06/13)

The present invention relates to a method for preparing S-HGB ((S)-3-hydroxy-γ-butyrolactone) using hydrolase, and more particularly to a method for preparing S-HGB in a high purity by hydrolyzing S-BBL ((S)-β-benzoyloxy-γ-butyrolactone) in the presence of hydrolase. According to the present invention, the S-HGB having an optical purity can be obtained in a high yield under simple process conditions without requiring reaction conditions of high pressure and high temperature or complex operation conditions by hydrolyzing S-BBL with hydrolase.

Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety

Vi?a, Dolores,Wu, Tongfei,Renders, Marleen,Laflamme, Geneviève,Herdewijn, Piet

, p. 2634 - 2646 (2007/10/03)

A synthetic scheme has been developed for the synthesis of 2′-deoxythreose phosphonate nucleosides from β-hydroxy-γ-butyrolactone and of 2′-azido erythrose phosphonate nucleosides from dihydroxydihydrofuran-1-one. In addition several α-l-arabinofuranose p

PHOSPONATE NUCLEOSIDES USEFUL AS ACTIVE INGREDIENTS IN PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF VIRAL INFECTIONS, AND INTERMEDIATES FOR THEIR PRODUCTION

-

Page/Page column 98, (2010/02/14)

The present invention relates to novel phosponate nucleosides, more specifically to novel phosponalkoxy substituted nucleosides. The invention further relates to compounds having HIV (Human Immunodeficiency Virus) replication inhibiting properties and to

Beta-substituted-gamma-butyrolactones and a process for preparation thereof

-

Page 6, (2008/06/13)

The present invention is related to a process for the preparation of (S)- or (R)-β-substituted-γ-butyrolactones or a racemic mixture thereof. β-substituted-γ-succinic anhydrides are converted by zinc borohydride in a compatible solvent selected from tetra

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