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2942-45-2

2942-45-2

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2942-45-2 Usage

Type of Compound

Heterocyclic compound

Derivative

Pyrazole

Usage

Research chemical

Potential Pharmacological Effects

a. Anti-inflammatory
b. Analgesic agent

Investigation for Treatment

a. Neurological disorders

Research Status

Relative novelty, limited research, and properties/applications still being explored.

Check Digit Verification of cas no

The CAS Registry Mumber 2942-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2942-45:
(6*2)+(5*9)+(4*4)+(3*2)+(2*4)+(1*5)=92
92 % 10 = 2
So 2942-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O/c1-10-6-5(7(11)9-10)3-2-4-8-6/h2-4H,1H3,(H,9,11)

2942-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2H-pyrazolo[3,4-b]pyridin-3-one

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-1-methyl-1H-pyrazolo<3,4-b>pyridin

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:2942-45-2 SDS

2942-45-2Downstream Products

2942-45-2Relevant articles and documents

A general, one-step synthesis of substituted indazoles using a flow reactor

Wheeler, Rob C.,Baxter, Emma,Campbell, Ian B.,MacDonald, Simon J. F.

experimental part, p. 565 - 569 (2011/12/02)

Flow chemistry is a rapidly emerging technology within the pharmaceutical industry, both within medicinal and development chemistry groups. The advantages of flow chemistry, increased safety, improved reproducibility, enhanced scalability, are readily apparent, and we aimed to exploit this technology in order to provide small amounts of pharmaceutically interesting fragments via a safe and scalable route, which would enable the rapid synthesis of multigram quantities on demand. Here we report a general and versatile route which utilises flow chemistry to deliver a range of known and novel indazoles, including 3-amino and 3-hydroxy analogues.

Synthesis and biological activity of pyrazo-[3,4-b]-pyridine derivatives. Part I

Kuczynski,Mrozikiewicz,Banaszkiewicz,Poreba

, p. 217 - 225,219,220,221 (2007/10/08)

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