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92295-43-7

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92295-43-7 Usage

General Description

1-(6-Methylpyridin-3-yl)ethanamine is a chemical compound with the molecular formula C8H12N2. It is also known as 6-methyl-3-pyridylethylamine or 6-methylpicolylethylamine. This chemical is an amine, which means it contains a nitrogen atom bonded to at least one alkyl group. It is used in the pharmaceutical industry for the synthesis of various drugs and as a building block for other organic compounds. 1-(6-Methylpyridin-3-yl)ethanamine has a range of potential applications, including as a precursor for the production of various pharmaceuticals and as an intermediate in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 92295-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,9 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92295-43:
(7*9)+(6*2)+(5*2)+(4*9)+(3*5)+(2*4)+(1*3)=147
147 % 10 = 7
So 92295-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-6-3-4-8(5-10-6)7(2)9/h3-5,7H,9H2,1-2H3

92295-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-methylpyridin-3-yl)ethanamine

1.2 Other means of identification

Product number -
Other names 1-(6-methyl-3-pyridinyl)ethanamine

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:92295-43-7 SDS

92295-43-7Downstream Products

92295-43-7Relevant articles and documents

Effective conversion of heteroaromatic ketones into primary amines via hydrogenation of intermediate ketoximes

Baucom, Kyle D.,Guram, Anil S.,Borths, Christopher J.

supporting information, p. 201 - 204 (2015/03/03)

A process to access heteroaromatic primary amines from the corresponding heteroaromatic ketones has been developed. A broad range of previously reported methods to convert ketones to primary amines was examined on heterocyclic ketones without success, including Leuckart-Wallach conditions, borane reductions, and transition-metal-catalyzed hydrogenations. Unique among the catalysts examined, Raney cobalt produced the desired primary heterocyclic amine. Raney cobalt hydrogenation of structurally varied heterocyclic ketoximes was demonstrated to form primary amines in good selectivity under mild conditions, and the products are easily isolated in high yield. Additionally, this is the first report of a systematic evaluation of the capabilities of Raney cobalt as an oxime hydrogenation catalyst.

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