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296276-41-0

296276-41-0

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296276-41-0 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 296276-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,2,7 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 296276-41:
(8*2)+(7*9)+(6*6)+(5*2)+(4*7)+(3*6)+(2*4)+(1*1)=180
180 % 10 = 0
So 296276-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H10F3N/c1-13-6-7-4-2-3-5-8(7)9(10,11)12/h2-5,13H,6H2,1H3

296276-41-0SDS

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 N-methyl-1-[2-(trifluoromethyl)phenyl]methanamine

1.2 Other means of identification

Product number -
Other names N-Methyl-2-trifluoromethylbenzylamine

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:296276-41-0 SDS

296276-41-0Downstream Products

296276-41-0Relevant articles and documents

SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF

-

Paragraph 00513, (2018/08/03)

Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.

FLUORINE-CONTAINING BENZALDEHYDES IN THE LEUCKART AND RODIONOV REACTIONS

Kolycheva, M. T.,Gerus, I. I.,Kukhar, V. P.

, p. 2134 - 2138 (2007/10/02)

Benzaldehydes containing polyfluoroalkoxy groups in the aromatic ring give the respective N-formylbenzamines by the action of formamide under the conditions of the Leuckart reaction.The products are converted by hydrolysis into benzylamines, while reducti

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