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1H-Pyrazolo[3,4-c]pyridazin-3-amine is a heterocyclic compound characterized by a pyrazolo[3,4-c]pyridazine ring system, which consists of a pyrazole and a pyridazine fused together. This nitrogen-containing molecule is an important building block in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties. It is a white crystalline solid with a molecular formula of C6H6N6 and a molecular weight of 162.16 g/mol. The compound is known for its potential applications in the development of new drugs, particularly those targeting the central nervous system, as well as its use in the creation of novel materials with specific properties.

2125-94-2

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2125-94-2 Usage

Compound class

pyrazolo[3,4-c]pyridazine

Structural characteristic

a pyrazole ring fused with a pyridazine ring

Derivative of

3-aminopyrazole

Potential applications

pharmaceutical research, drug development for various diseases and conditions

Relevance

organic synthesis, materials science

Check Digit Verification of cas no

The CAS Registry Mumber 2125-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2125-94:
(6*2)+(5*1)+(4*2)+(3*5)+(2*9)+(1*4)=62
62 % 10 = 2
So 2125-94-2 is a valid CAS Registry Number.

2125-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-Pyrazolo[3,4-c]pyridazin-3-amine

1.2 Other means of identification

Product number -
Other names 1H-Pyrazolo<3,4-b>pyrazin

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:2125-94-2 SDS

2125-94-2Downstream Products

2125-94-2Relevant academic research and scientific papers

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

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Page/Page column 168, (2017/12/28)

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.

ALKYNYL ALCOHOLS AND METHODS OF USE

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Page/Page column 409, (2015/03/13)

The invention relates to compounds of Formula (0): wherein Q, A1-A8, R4 and R5 and each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over- activation of NF-kB signaling is observed.

Synthesis of Pyridazine Derivatives through the Unexpected Intermediate 5-Amino-4-Cyano-2,3-Dihydro-Furan-2,3-Disulfonic Acid Disodium Salt

Cacciari, Barbara,Spalluto, Giampiero,Ferretti, Valeria

, p. 1065 - 1069 (2007/10/03)

An unexpected compound (5-amino-4-cyano-2,3-dihydrofuran-2,3-disulfonic acid disodium salt, 4) was isolated from the reaction of glyoxale bis hydrogen sulfite disodium salt with malononitrile. Its structure was undoubtly identified through crystal structure analysis. Compound 4 was highly stable and it was isolated easily and in a very high yield. Its reactivity was studied in the reactions with some hydrazine derivatives in order to obtain different pyridazine analogs.

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