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1H-Imidazo[4,5-c]pyridazine is a heterocyclic compound characterized by a fused imidazole and pyridazine ring system. This chemical structure is of interest in medicinal chemistry due to its potential applications in the development of pharmaceuticals, particularly as a scaffold for designing new drugs. The compound's unique arrangement of nitrogen atoms in the ring system can facilitate the formation of various biologically active molecules. Research into 1H-imidazo[4,5-c]pyridazine and its derivatives may lead to the discovery of new therapeutic agents with diverse mechanisms of action, making it a significant area of study in the field of drug discovery and development.

327-02-6

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327-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 327-02-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 327-02:
(5*3)+(4*2)+(3*7)+(2*0)+(1*2)=46
46 % 10 = 6
So 327-02-6 is a valid CAS Registry Number.

327-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5(7)H-imidazo[4,5-c]pyridazine

1.2 Other means of identification

Product number -
Other names Imidazo[4,5-c]pyridazin

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:327-02-6 SDS

327-02-6Downstream Products

327-02-6Relevant academic research and scientific papers

An efficient hetero Diels-Alder approach to imidazo[4,5-c]pyridazines as purine analogues

Deghati, Paymaneh Y.F.,Wanner, Martin J.,Koomen, Gerrit-Jan

, p. 4561 - 4564 (2007/10/03)

A general approach to 3-deaza-6-azapurine by a hetero Diels-Alder reaction is described. Reaction of sulfonamide protected 5-vinylimidazole with 4-phenyl-1,2,4-triazoline-3,5-dione in methanol gave the Diels-Alder adduct 8 in 85% yield. Deprotection of the resulting N-phenyltriazole was efficiently accomplished by ring opening with hydrazine followed by heating in DMSO. The completely deprotected and aromatized purine analogue 1 was obtained directly from this one-pot reaction in 48% yield.

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