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6-(4-chlorophenyl)-3-nitro-2-Pyridinamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102291-55-4

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102291-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102291-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,9 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102291-55:
(8*1)+(7*0)+(6*2)+(5*2)+(4*9)+(3*1)+(2*5)+(1*5)=84
84 % 10 = 4
So 102291-55-4 is a valid CAS Registry Number.

102291-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-6-(4-chlorphenyl)-3-nitropyridin

1.2 Other means of identification

Product number -
Other names 6-(4-chlorophenyl)-3-nitropyridin-2-ylamine

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:102291-55-4 SDS

102291-55-4Downstream Products

102291-55-4Relevant academic research and scientific papers

TRIAZOLOPYRIDINE CARBOXAMIDE DERIVATIVES AND TRIAZOLOPYRIMIDINE CARBOXAMIDE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

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Page/Page column 3-4, (2010/03/04)

The invention relates to the triazolopyridine carboxamide derivatives and triazolopyrimidine carboxamide derivatives of general formula (I): Wherein X, A, R1 and R2 are as defined herein. The invention further relates to preparation methods and therapeutic use thereof.

Synthesis of 2-Amino-3-nitropyridines and -1,4-dihydropyridines

Mertens, Hubert,Troschuetz, Reinhard,Roth, Hermann J.

, p. 380 - 383 (2007/10/02)

The title compounds 4 and 5 can be synthesized from the primary nitroketene aminal 2 and 1,3-biselectrophiles like β-aminoketones (ketonic Mannich bases) or enaminoketones.

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