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34008-93-0

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34008-93-0 Usage

Physical state

Colorless liquid

Odor

Mildly sweet

Uses

Intermediate in organic synthesis, solvent in industrial applications

Flammability

Flammable

Volatility

Low

Applications

Synthesis of pharmaceuticals, agrochemicals, and fine chemicals

Role in organic reactions

Reagent, coupling agent, and catalyst

Safety precautions

Can cause skin, eye, and respiratory irritation; handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 34008-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,0 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34008-93:
(7*3)+(6*4)+(5*0)+(4*0)+(3*8)+(2*9)+(1*3)=90
90 % 10 = 0
So 34008-93-0 is a valid CAS Registry Number.

34008-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethylsulfonyl-2-methylpropane

1.2 Other means of identification

Product number -
Other names HMS1703N05

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:34008-93-0 SDS

34008-93-0Upstream product

34008-93-0Downstream Products

34008-93-0Relevant articles and documents

PROCESS FOR PREPARATION OF ALKYL SULFONE COMPOUNDS

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Page/Page column 7, (2012/05/04)

An object of the present invention is to provide a method for preparation of an alkyl sulfone compound simply and safely with high yield, and an alkyl sulfone compound. The present invention is a method for preparing an alkyl sulfone compound represented by formula (2), comprising: oxidizing an alkyl sulfide compound represented by formula (1) using an oxidizing agent in the presence of a tungstate catalyst: in formula (1), R1 represents a C1-C3 alkyl group, and R2 represents a C3-C5 alkyl group, in formula (2), R1 and R2 are the same alkyl groups as R1 and R2 in formula (1), respectively.

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