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1H-Pyrazolo[4,3-b]pyridine-3-carboxamide, 6-nitro-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88796-41-2

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88796-41-2 Usage

Compound class

pyrazolo[4,3-b]pyridine

Contains

nitro group, phenyl group

Usage

pharmaceutical synthesis, drug intermediate

Potential

biological activities, therapeutic properties

Precaution

health and environmental hazards

Check Digit Verification of cas no

The CAS Registry Mumber 88796-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88796-41:
(7*8)+(6*8)+(5*7)+(4*9)+(3*6)+(2*4)+(1*1)=202
202 % 10 = 2
So 88796-41-2 is a valid CAS Registry Number.

88796-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-1-phenylpyrazolo[4,3-b]pyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Pyrazolo[4,3-b]pyridine-3-carboxamide,6-nitro-1-phenyl

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:88796-41-2 SDS

88796-41-2Downstream Products

88796-41-2Relevant academic research and scientific papers

5,6-CONDENSED 3-NITROPYRIDINES FROM HETEROCYCLIC AMINES AND NITROMALONALDEHYDE

Schaefer, H.,Gewald, K.,Schmidt, M.

, p. 1163 - 1166 (2007/10/02)

The reaction of nitromalonaldehyde with 2-aminothiophenes leads to 5-nitrothienopyridines.The analogous reaction with 3-aminopyrroles leads to 6-nitropyrrolopyridines.The analogous reaction with 4- and 5-aminopyrazoles leads to 6-nitropyrazo

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