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2-Pentanone, 1,1,1-trifluoro-5-(2-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85674-69-7

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85674-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85674-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,7 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85674-69:
(7*8)+(6*5)+(5*6)+(4*7)+(3*4)+(2*6)+(1*9)=177
177 % 10 = 7
So 85674-69-7 is a valid CAS Registry Number.

85674-69-7SDS

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 1,1,1-trifluoro-5-(2-methylphenyl)pentan-2-one

1.2 Other means of identification

Product number -
Other names 5-(o-tolyl)-1,1,1-trifluoro-2-pentanone

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:85674-69-7 SDS

85674-69-7Relevant academic research and scientific papers

Syntheses of 1-trifluoromethyl-2-naphthalenols via a novel construction of the naphthalene nucleus

Fung, Steven,Abraham, Nedumparambil A.,Bellini, Francesco,Sestanj, Kazimir

, p. 368 - 371 (2007/10/02)

A relative simple and efficient synthesis of the hitherto unknown 1-trifluoromethyl-2-naphthalenols is described.Easily acsessible benzoid precursors 6 and 7 were converted to the oximino-ketones 8 and 9 by nitrosation.A novel cyclization and hydrolysis a

6-(Lower alkoxy)-5-(trifluoromethyl)-1-naphthalenecarboxaldehydes

-

, (2008/06/13)

A process and intermediates for preparing 6-(lower alkoxy)-5-(trifluoromethyl)-1-naphthalenecarboxylic acid derivatives are disclosed. The derivatives are useful for preparing aldose reductase inhibitors. With reference to the process, 1,1,1-trifluoro-5-(2-methylphenyl)-2,3-pentadione 3-oxime is cyclized to give a key intermediate 3,4-dihydro-1-hydroxy-5-methyl-1-(trifluoromethyl)-2(1H)-naphthalenone oxime; and 3,4-dihydro-1-hydroxy-5-methyl-1-(trifluoromethyl)-2(1H)-naphthalenone is aromatized to 5-methyl-1-(trifluoromethyl)-2-naphthalenol with a dehydrating agent.

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