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Benzenemethanol, α-methyl-2-(methylthio)-, also known as 2-(methylthio)-α-methylbenzenemethanol or 2-(methylthio)-α-methylbenzyl alcohol, is an organic compound with the chemical formula C9H12OS. It is a colorless to pale yellow liquid with a molecular weight of 164.26 g/mol. Benzenemethanol, a-methyl-2-(methylthio)- is characterized by the presence of a benzene ring with a methyl group attached to the α-carbon of a benzyl alcohol moiety, and a methylthio group at the 2-position. It is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it can undergo a range of chemical transformations, making it a valuable building block in organic synthesis.

30439-31-7

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30439-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30439-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,3 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30439-31:
(7*3)+(6*0)+(5*4)+(4*3)+(3*9)+(2*3)+(1*1)=87
87 % 10 = 7
So 30439-31-7 is a valid CAS Registry Number.

30439-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-(methylthio)phenyl)ethanol

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:30439-31-7 SDS

30439-31-7Relevant academic research and scientific papers

Preparation of chiral organochalcogeno-α-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root

Comasseto, Jo?o V.,Omori, álvaro T.,Porto, André L. M.,Andrade, Leandro H.

, p. 473 - 476 (2007/10/03)

A series of organochalcogeno acetophenones 3 has been submitted to the action of enzymes from Daucus carota root. Some of the chalcogeno ketones tested afforded the chiral organochalcogeno-α-methylbenzyl alcohols 4 in excellent enantiomeric excesses (>99%), under mild and environmentally friendly conditions. The stereoselectivity of the reduction is in accordance with Prelog's rule. Enzymatic kinetic resolution as alternative process was used to obtain the chiral ortho-organochalcogeno-α-methylbenzyl alcohols in excellent enantiomeric excess (>99%).

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