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1-chloro-3-(octylsulfanyl)propan-2-ol is a chemical compound with the molecular formula C11H23ClO2S. It is an alcohol derivative with a chlorine atom attached to the first carbon, a hydroxyl group attached to the second carbon, and a thioether group attached to the third carbon of the propane backbone.

4542-56-7

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4542-56-7 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-chloro-3-(octylsulfanyl)propan-2-ol is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and potential biological activity.
Used in Organic Synthesis:
1-chloro-3-(octylsulfanyl)propan-2-ol is used as a solvent or intermediate in organic synthesis, facilitating various chemical reactions.
Used in Disinfectants and Antiseptics:
1-chloro-3-(octylsulfanyl)propan-2-ol is used as a mild antimicrobial agent in the formulation of disinfectants and antiseptics, providing a potential alternative for sanitizing applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4542-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4542-56:
(6*4)+(5*5)+(4*4)+(3*2)+(2*5)+(1*6)=87
87 % 10 = 7
So 4542-56-7 is a valid CAS Registry Number.

4542-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-octylsulfanylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 3-Chlor-2-hydroxypropyl-n-octylsulfid

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:4542-56-7 SDS

4542-56-7Downstream Products

4542-56-7Relevant academic research and scientific papers

Halohydrin thioethers

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, (2008/06/13)

Compounds of the structure R(SCH2 CHOHCH2 X)n when n=1 to 4 and R is a hydrocarbon, ether, ester, acetal, hydroxy aliphatic, hydroxy aromatic, imide or amide group or halogenated derivatives thereof are prepared by reacting 1-halo-3-mercapto-2-propanol with an aliphatically unsaturated compound using free radical initiators as catalysts. The compounds in which R is an unsaturated or polyunsaturated aliphatic hydrocarbon group of 2 to 24 carbon atoms, or an unsaturated or polyunsaturated cycloaliphatic group, and those in which the aliphatic or cycloaliphatic group is connected through two or more of the polyunsaturated to two or more --S--CH2 CHOHCHCl groups, and compounds where R is an alkylene or polyalkylene substituted aromatic group and the hydroxy, thioalkyl, alkoxy, aryloxy, ester, carbamidoalkyl and sulfamidoalkyl, halogenated derivatives of said groups are new compounds. The thioether halohydrins can be converted to epoxides. The process utilizing a radioactive energy source as a catalyst is new.

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