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165558-80-5

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165558-80-5 Usage

General Description

N-methyl-1-(2-(trifluoromethyl)pyridin-4-yl)methanamine is a chemical compound that contains a methyl group, a pyridine ring with a trifluoromethyl substituent, and a methanamine group. It belongs to the class of organic compounds known as phenylmethylamines. N-methyl-1-(2-(trifluoromethyl)pyridin-4-yl)methanamine has potential applications in pharmaceuticals and research due to its unique structure and potential biological activities. It is important to handle this chemical with care, following proper safety protocols and guidelines for handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 165558-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,5,5 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 165558-80:
(8*1)+(7*6)+(6*5)+(5*5)+(4*5)+(3*8)+(2*8)+(1*0)=165
165 % 10 = 5
So 165558-80-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H9F3N2/c1-12-5-6-2-3-13-7(4-6)8(9,10)11/h2-4,12H,5H2,1H3

165558-80-5SDS

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)pyridin-4-yl]methanamine

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:165558-80-5 SDS

165558-80-5Downstream Products

165558-80-5Relevant articles and documents

Preparation of benzindole compounds from naphthalene compounds

-

, (2008/06/13)

The invention relates to a process for preparing a substituted 2-amino-benz[cd]indole of the Formula I: STR1 The nitro group of a substituted 1-nitro-8-cyano-naphthalene compound is reduced to an amine group to form a substituted 1-amino-8-cyano-naphthalene compound, which is cyclized to form the substituted 2-amino-benz[cd]indole. The reduction and cyclization may be effected in a one-pot procedure using a reducing agent such as stannous chloride, which generates an acid that cyclizes the reduction product. The syntheses of the 1-nitro-8-cyanonaphthalene compound and its precursors are also described.

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