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4-(1H-PYRAZOL-4-YL)PYRIDINE, with the CAS number 185112-61-2, is an important organic compound characterized by its molecular formula of C9H8N2. It is known for its pyrazole and pyridine rings, which enable a variety of chemical reactions, making it a valuable building block in chemical synthesis. 4-(1H-PYRAZOL-4-YL)PYRIDINE is typically found as a pale yellow to off-white crystalline powder and should be stored in a cool, dry place to ensure its stability. Due to potential safety hazards, it is essential to handle 4-(1H-PYRAZOL-4-YL)PYRIDINE with care.

19959-71-8

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19959-71-8 Usage

Uses

Used in Pharmaceutical Industry:
4-(1H-PYRAZOL-4-YL)PYRIDINE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 4-(1H-PYRAZOL-4-YL)PYRIDINE serves as a key building block for the creation of complex molecules. Its pyrazole and pyridine rings facilitate diverse chemical reactions, contributing to the advancement of chemical knowledge and the discovery of new compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 19959-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19959-71:
(7*1)+(6*9)+(5*9)+(4*5)+(3*9)+(2*7)+(1*1)=168
168 % 10 = 8
So 19959-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3/c1-3-9-4-2-7(1)8-5-10-11-6-8/h1-6H,(H,10,11)

19959-71-8SDS

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 4-(1H-Pyrazol-4-yl)pyridine

1.2 Other means of identification

Product number -
Other names -

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:19959-71-8 SDS

19959-71-8Relevant academic research and scientific papers

Design, synthesis, and biologic evaluation of some novel N-arylpyrazole derivatives as cytotoxic agents

Xu, Shengjie,Li, Shenghui,Tang, Yonghe,Zhang, Jinchao,Wang, Shuxiang,Zhou, Chuanqi,Li, Xiaoliu

, p. 5610 - 5616 (2013/12/04)

A novel series of N-arylpyrazole derivatives (5a-5d, 7a-7c) has been designed and synthesized via aromatic substitution reaction of N-nonsubstituted pyrazoles with 4-fluoronitrobenzene in the presence of base. The structures of these compounds were establ

A simple and environmentally benign synthesis of polypyridine- polycarboxylic acids

Kelly, Niamh R.,Goetz, Sandrine,Hawes, Chris S.,Kruger, Paul E.

scheme or table, p. 995 - 998 (2011/03/21)

An oxidation method using dilute nitric acid solutions under solvothermal conditions has been developed to synthesise a series of polypyridine- polycarboxylic acids. It has been successfully applied to a range of methyl substituted polypyridines including symmetrical and asymmetrical 2,2′-bipyridines; 2,2′:6′,2″-terpyridines and; 2,2′:6′,2″:6″,2?-tetra-pyridines and yields crystalline polypyridine-polycarboxylic acids in a single step. Simple product recovery through filtration yields a recyclable filtrate. More forcing conditions led to demethylation of the polypyridine ligand most probably via decarboxylation. This simple approach avoids potentially harmful metal-based oxidants and negates any issues associated with the disposal of their resultant (hazardous) waste.

HETEROARYLPIPERIDINE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

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Page 63, (2008/06/13)

The present invention is directed to compounds of the formula (I): (wherein R>12345610 and n are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.

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