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4-phenylsulfonyl-5-prop-1-enyl-tetrahydrofuran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112751-90-3

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112751-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112751-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,5 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112751-90:
(8*1)+(7*1)+(6*2)+(5*7)+(4*5)+(3*1)+(2*9)+(1*0)=103
103 % 10 = 3
So 112751-90-3 is a valid CAS Registry Number.

112751-90-3SDS

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 4-phenylsulfonyl-5-prop-1-enyl-tetrahydrofuran-2-one

1.2 Other means of identification

Product number -
Other names -

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:112751-90-3 SDS

112751-90-3Relevant academic research and scientific papers

Synthesis and structural study of (+)-5-acetyl-6-methyl-5p-tolylsulfinyl- 3a,4,5,6-tetrahydro (3H)-benzofuran-2-one

Alexandre,Belkadi,Rouessac

, p. 447 - 452 (2007/10/02)

An efficient synthesis of the title compound has been developed from 3- phenyl sulfonylpropanoic acid via the butenolide 2. The key synthetic step is a Diels-Alder reaction. A mechanism is suggested.

METHYL 3-PHENYLSULPHONYL ORTHOPROPIONATE: AN EFFICIENT REAGENT FOR THE SYNTHESIS OF γ-LACTONES AND BUTENOLIDES

Carretero, Juan Carlos,Lombaert, Stephane De,Ghosez, Leon

, p. 2135 - 2138 (2007/10/02)

Treatment of methyl 3-phenylsulphonyl orthopropionate with n-BuLi gives the corresponding carbanion which reacts with aldehydes or ketones to yield β-phenylsulphonyl-γ-lactones.Base-catalysed elimination yields α,β or β,γ-butenolides.

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