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75462-61-2

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75462-61-2 Usage

General Description

3,5-Bis(trifluoromethyl)toluene, also known as perfluoro-1,3,5-trimethylbenzene, is a chemical compound with the molecular formula C9H6F6. It is a colorless liquid with a fruity odor and is commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and dyes. It is also used as a solvent and as a reagent in organic synthesis. 3,5-Bis(trifluoromethyl)toluene is known for its high thermal stability and chemical inertness, making it a valuable compound in various industrial applications. However, it is important to handle this chemical with care as it can be harmful if swallowed, inhaled, or in contact with skin, and may cause irritation to the eyes and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 75462-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,6 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75462-61:
(7*7)+(6*5)+(5*4)+(4*6)+(3*2)+(2*6)+(1*1)=142
142 % 10 = 2
So 75462-61-2 is a valid CAS Registry Number.

75462-61-2SDS

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-methyl-3,5-bis(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names Dtfmbzbr

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:75462-61-2 SDS

75462-61-2Relevant articles and documents

Selective cleavage of 3,5-bis-(trifluoromethyl)benzylcarbamate by SmI 2-Et3N-H2O

Ankner, Tobias,Said Stalsmeden, Anna,Hilmersson, Goeran

, p. 6867 - 6869 (2013/07/26)

A novel electron poor protection group for amines has been developed. It undergoes rapid cleavage by SmI2-Et3N-H2O and its orthogonality towards the regular benzyl carbamate group (CBz) under reductive or transfer hydrogenolytic conditions is reported.

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