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4,7-Diaza-1H-indazole, also known as 2,3-diaza-4H-cinnoline, is a heterocyclic compound characterized by its bicyclic structure with two nitrogen atoms within the fused ring system. As a derivative of indazole, this weak base has garnered interest in the fields of coordination chemistry and organic synthesis. Its potential pharmacological activities, particularly its antitumor and antimicrobial properties, have made it a subject of scientific investigation.

272-60-6

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272-60-6 Usage

Uses

Used in Pharmaceutical Industry:
4,7-Diaza-1H-indazole is used as a precursor in the synthesis of various organic compounds for pharmaceutical applications due to its unique chemical structure and potential pharmacological activities.
Used in Coordination Chemistry:
4,7-Diaza-1H-indazole is used as a ligand in coordination chemistry, where its ability to form stable complexes with metal ions contributes to the development of new materials with specific properties.
Used in Antitumor Applications:
4,7-Diaza-1H-indazole is used as a potential antitumor agent, with ongoing research exploring its effects on tumor growth and progression, as well as its potential synergistic effects with conventional chemotherapeutic drugs.
Used in Antimicrobial Applications:
4,7-Diaza-1H-indazole is used as a potential antimicrobial agent, with studies investigating its ability to inhibit the growth of various microorganisms, offering a new avenue for the development of antimicrobial drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 272-60-6 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 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 272-60:
(5*2)+(4*7)+(3*2)+(2*6)+(1*0)=56
56 % 10 = 6
So 272-60-6 is a valid CAS Registry Number.

272-60-6SDS

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 1H-pyrazolo[3,4-b]pyrazine

1.2 Other means of identification

Product number -
Other names 1(2)H-pyrazolo[3,4-b]pyrazine

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:272-60-6 SDS

272-60-6Downstream Products

272-60-6Relevant academic research and scientific papers

PYRIDINE AND PYRIMIDINE DERIVATIVES AND THEIR USE IN TREATMENT, AMELIORATION OR PREVENTION OF INFLUENZA

-

, (2017/09/02)

Provided herein is a compound of formula (I), optionally in the form of a pharmaceutically acceptable salt, solvate, polymorph, prodrug, codrug, cocrystal, tautomer, racemate, enantiomer,or diastereomer or mixture thereof, which is useful in treating, ameliorating or preventing influenza.

Neighbouring Group Participation in Formation of Condensed Azines. Formation of Pyrazolo(3,4-b)pyrazines, Isoxazolo(4,5-b)pyrazines and Isothiazolo(5,4-b)pyridine (Heterocycles, CCX)

Kocevar, Marjan,Vercek, Bojan,Stanovnik, Branko,Tisler, Miha

, p. 731 - 744 (2007/10/02)

Pyrazine- and pyridinecarboxamidoximes with an amino, potentially tautomeric hydroxy or mercapto group in ortho position could be transformed in the appropriate condensed azines.In this manner, representatives of pyrazolo(3,4-b)pyrazine, isoxazolo(4,5-b)pyrazine and isothiazolo(5,4-b)pyridine ring system were synthesized and some transformations investigated. - Keywords: Cyclization with N-N, N-O or N-S bond formation; Heterocyclic compounds

NEW SYNTHETIC APPROACH FOR PYRAZOLOPYRAZINES AND ISOXAZOLOPYRAZINES

Kocevar, Marjan,Tisler, Miha,Stanovnik, Branko

, p. 339 - 342 (2007/10/02)

A new synthetic approach has been developed for the synthesis of pyrazolepyrazines (7) and isoxazolopyrazines (22) from the corresponding substituted pyrazines.

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