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103659-47-8

Benzenepropanol, a-methyl-a-(trichloromethyl)-, also known as 2-(2,2,2-trichloro-1-hydroxyethyl)-1-methylbenzene, is an organic compound with the chemical formula C10H11Cl3O. It is a colorless liquid with a molecular weight of 259.56 g/mol. Benzenepropanol, a-methyl-a-(trichloromethyl)- is characterized by the presence of a benzene ring, a propanol group, and a trichloromethyl group. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its potential health and environmental risks, handling and disposal of this chemical should be done with proper safety measures and in accordance with local regulations.

103659-47-8

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103659-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103659-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,5 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103659-47:
(8*1)+(7*0)+(6*3)+(5*6)+(4*5)+(3*9)+(2*4)+(1*7)=118
118 % 10 = 8
So 103659-47-8 is a valid CAS Registry Number.

103659-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trichloro-2-hydroxy-2-methyl-4-phenylbutane

1.2 Other means of identification

Product number -
Other names 1,1,1-trichloro-2-methyl-4-phenylbutan-2-ol

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:103659-47-8 SDS

103659-47-8Relevant articles and documents

An improved preparation and a new application of trichloromethylcarbinols from enolizable ketones

Li, Jing,Derstine, Brenden,Itoh, Takahiro,Balsells, Jaume

supporting information, p. 3151 - 3153 (2014/05/20)

We report an improved method for the preparation of trichloromethylcarbinols from enolizable ketones. Trichloromethylcarbinols were obtained in good to excellent yields by using of a combination of CHCl 3, n-BuLi, and chlorotitanium (IV) triiso

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