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114232-68-7

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114232-68-7 Usage

Classification

Thioether

Physical state

Colorless liquid

Odor

Strong, unpleasant

Flammability

Flammable

Industrial applications

Used as a chemical intermediate in the production of other chemicals

Handling and storage

Should be handled and stored with caution due to potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 114232-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,3 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114232-68:
(8*1)+(7*1)+(6*4)+(5*2)+(4*3)+(3*2)+(2*6)+(1*8)=87
87 % 10 = 7
So 114232-68-7 is a valid CAS Registry Number.

114232-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1,2-di(ethylthio)-1-propene

1.2 Other means of identification

Product number -
Other names 1,2-bis(ethylthio)propene

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:114232-68-7 SDS

114232-68-7Downstream Products

114232-68-7Relevant articles and documents

REACTION OF Α-CHLORO KETONES WITH THIOLS

Mursakulov, I. G.,Ramazanov, E. A.,Kerimov, F. F.,Abbasov, I. M.,Zefirov, N. S.

, p. 1416 - 1425 (2007/10/02)

The reaction of α-chloro ketones with ethane-, propane-, and butanethiols leads to the corresponding (alkylthio)alkenes.Noncyclic chloro ketones give a mixture of the cis and trans isomers of di(alkylthio)alkenes, while the reaction of α-chloropinacoline leads only to the cis isomers of the 1,2-di(alkylthio)-3,3-dimethyl-1-butene.The mechanism of the reaction of α-chloro ketones with thiols includes nucleophilic substitution of the chlorine with the formation of alkylthio ketones.The addition of a further molecule leads to the corresponding intermediate alkylthio a cohols, which are easily dehydrated to the final products under the acidic conditions.

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