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274-85-1

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274-85-1 Usage

Description

1,7,9-Triazabicyclo[4.3.0]nona-2,4,6,8-tetraene is a heterocyclic compound characterized by its unique bicyclic structure and the presence of three nitrogen atoms in its ring system. It is known for its potential applications in various chemical and pharmaceutical processes due to its reactive nature and structural properties.

Uses

Used in Chemical Synthesis:
1,7,9-Triazabicyclo[4.3.0]nona-2,4,6,8-tetraene is used as a key reactant in the synthesis of various complex organic compounds, particularly in the formation of triazoloquinoline derivatives. Its unique structure allows for the creation of novel molecules with potential applications in different fields.
Used in Pharmaceutical Industry:
1,7,9-Triazabicyclo[4.3.0]nona-2,4,6,8-tetraene is used as an intermediate in the development of new pharmaceutical compounds. Its reactivity and structural diversity make it a valuable building block for designing and synthesizing novel drugs with improved therapeutic properties.
Used in Research and Development:
In the field of research and development, 1,7,9-triazabicyclo[4.3.0]nona-2,4,6,8-tetraene serves as a versatile compound for exploring new reaction pathways and understanding the fundamental chemistry of heterocyclic systems. Its unique properties can lead to the discovery of new synthetic methods and applications in various industries.

Synthesis Reference(s)

Tetrahedron Letters, 14, p. 1677, 1973 DOI: 10.1016/S0040-4039(01)96026-5

Check Digit Verification of cas no

The CAS Registry Mumber 274-85-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 274-85:
(5*2)+(4*7)+(3*4)+(2*8)+(1*5)=71
71 % 10 = 1
So 274-85-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H5N3/c1-2-4-9-6(3-1)7-5-8-9/h1-5H

274-85-1SDS

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 [1,2,4]Triazolo[1,5-a]pyridine

1.2 Other means of identification

Product number -
Other names [1,2,4]triazolo[1,5-a]pyridine

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:274-85-1 SDS

274-85-1Relevant articles and documents

A New Synthesis of the s-Triazolopyridine Ring System

Hajos, G.,Timari, G.,Messmer, A.,Zagyva, A.,Miskolczi, I.,Schantl, J. G.

, p. 1213 - 1216 (1995)

A novel and efficient synthesis of s-triazolopyridines was elaborated by reacting 1,2-diaminopyridinium salts with aldehydes. - Keywords: Ring closure; Triazoles, fused; Dipolar cycloaddition

FUNCTIONALIZED ENAMINES IN THE SYNTHESIS OF SOME HETEROCYCLIC COMPOUNDS

Golic, Ljubo,Stropnik, Crtomir,Stanovnik, Branko,Tisler, Miha

, p. 347 - 358 (2007/10/02)

Esters of 3-amino-2-cyanoacrylate and analogous compounds were used as starting material for pyridines which were obtained via the corresponding amidines.On the other hand, from ethyl 5-aminoisoxazole-4-carboxylate or 5-amino-4-cyanoisoxazole in a similar reaction sequence a pyrimidine derivative could be prepared.

SYNTHESES AND TRANSFORMATIONS OF SOME HETEROCYCLIC HYDROXYLAMINES

Tomazic, Alenka,Tisler, Miha,Stanovnik, Branko

, p. 1787 - 1794 (2007/10/02)

Syntheses of some hydroxylaminoazines, their quaternized derivatives or N-oxides and N-amino compounds are described.Several transformations of these compounds and cyclization reactions are presented.

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