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3-Pyridinecarbonitrile, 2-amino-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56162-65-3

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56162-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56162-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,6 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56162-65:
(7*5)+(6*6)+(5*1)+(4*6)+(3*2)+(2*6)+(1*5)=123
123 % 10 = 3
So 56162-65-3 is a valid CAS Registry Number.

56162-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-phenylpyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Amino-6-phenyl-3-pyridinecarbonitrile

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:56162-65-3 SDS

56162-65-3Downstream Products

56162-65-3Relevant academic research and scientific papers

1,8-NAPHTHYRIDINONE COMPOUNDS AND USES THEREOF

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Paragraph 0144; 0147, (2020/07/31)

1,8-naphthyridinone compounds as modulators of an adenosine receptor are provided. The compounds may find use as therapeutic agents for the treatment of diseases mediated through a G-protein-coupled receptor signaling pathway and may find particular use i

1,8-NAPHTHYRIDINONE COMPOUNDS AND USES THEREOF

-

, (2019/02/05)

1,8-naphthyridinone compounds as modulators of an adenosine receptor are provided. The compounds may find use as therapeutic agents for the treatment of diseases mediated through a G-protein-coupled receptor signaling pathway and may find particular use in oncology.

[5C + 1N] Annulation of 2,4-pentadienenitriles with hydroxylamine: A synthetic route to multi-substituted 2-aminopyridines

Xin, Xiaoqing,Huang, Peng,Xiang, Dexuan,Zhang, Rui,Zhao, Fengyu,Zhang, Ning,Dong, Dewen

, p. 1001 - 1006 (2013/02/26)

A facile and efficient synthetic route to multi-substituted 2-aminopyridines has been developed via a formal [5C + 1N] annulation of readily available 2,4-pentadienenitriles with hydroxylamine (NH2OH) under very mild conditions, which involves

Synthesis of substituted 2-aminonicotinonitriles

Troschutz,Dennstedt

, p. 33 - 40 (2007/10/02)

Mono-, di-, and trisubstituted 2-aminonicotinonitriles 8, 13, 14, and 19 are prepared from ketonic Mannich-bases hydrochlorides 4 · HCl, enones 12, β-aminovinylketones 17, 3-aminoacroleines 18, vinamidinium perchlorates 21, and 3,3-diaminoacrylonitrile (3

A New Route to 2-Amino- or 2-Hydroxy-3-pyridinecarboxylic Acid Derivatives

Ito, Kunio,Yokokura, Seiichi,Miyajima, Shingo

, p. 773 - 778 (2007/10/02)

Schiff's bases derived from ketones and t-butylamine (1) reacted with methyl methoxymethylenemalonate to give 2-hydroxy-3-pyridinecarboxylates.Similarly, treatment of 1 with ethoxymethylenemalononitrile gave 2-amino-3-pyridinecarbonitriles.Compounds 1 on reaction with ethyl 2-cyano-3-ethoxypropenoate afforded 2-amino-3-pyridinecarboxylates.

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