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7-Oxabicyclo[4.1.0]heptane, 2,2-dimethyl-5-[(phenylsulfonyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90020-49-8

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90020-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90020-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,2 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90020-49:
(7*9)+(6*0)+(5*0)+(4*2)+(3*0)+(2*4)+(1*9)=88
88 % 10 = 8
So 90020-49-8 is a valid CAS Registry Number.

90020-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonylmethylidene)-5,5-dimethyl-7-oxabicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names 2,3-epoxy-4,4-dimethylcyclohex-1-ylidenemethyl phenyl sulphone

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:90020-49-8 SDS

90020-49-8Downstream Products

90020-49-8Relevant academic research and scientific papers

Preparation of Vinylic Sulphones by Peterson Olefination using Phenyl Trimethylsilylmethyl Sulphone

Craig, Donald,Ley, Steven V.,Simpkins, Nigel S.,Whitham, Gordon H.,Prior, Michael J.

, p. 1949 - 1952 (2007/10/02)

The anion generated from phenyl trimethylsilylmethyl sulphone using butyl-lithium in dimethoxyethane, readily reacts at -78 deg C with various carbonyl compounds to afford vinylic sulphones on work-up at room temperature.The reaction conditions are tolera

Peterson Olefination using Phenylsulphonyltrimethylsilylmethane. A New Preparation of Vinylic Sulphones

Ley, Steven V.,Simpkins, Nigel S.

, p. 1281 - 1282 (2007/10/02)

The anion from phenylsulphonyltrimethylsilylmethane reacts, in 1,2-dimethoxyethane at -78 deg C, with both aldehydes and ketones to give the corresponding alkenyl phenyl sulphones in good yield.

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