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1H-Pyridazino[4,5-e][1,3,4]thiadiazine, 5-chloro-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96207-29-3

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96207-29-3 Usage

Chemical structure

A compound with a pyridazine ring fused to a thiadiazine ring.

Chlorine atom

Located at the 5-position of the compound.

Phenyl group

Attached at the 3-position of the compound.

Molecular weight

237.69 g/mol.

Potential pharmacological activity

May exhibit biological activity due to the presence of heterocyclic rings and a phenyl group.

Biological activity

Commonly found in many biologically active compounds.

Chemical reactivity

Influenced by the presence of the chlorine atom.

Applications

Possible uses in medicinal chemistry and drug discovery.

Further research

Necessary to fully understand the properties and potential uses of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 96207-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,0 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96207-29:
(7*9)+(6*6)+(5*2)+(4*0)+(3*7)+(2*2)+(1*9)=143
143 % 10 = 3
So 96207-29-3 is a valid CAS Registry Number.

96207-29-3Relevant academic research and scientific papers

Synthesis of Pyridazinothiadazines and the Ring Contraction to Pyrazolopyridazines through Extrusion of Sulfur

Kaji, Kenji,Nagashima, Hiromu,Nagao, Sigeto,Tabashi, Keizo,Oda, Hirohisa

, p. 4437 - 4446 (2007/10/02)

Cyclization of 2-substituted 5-4-chloro-3(2H)-pyridazinones (2) with potassium thioacetate, followed by deacetylation, provided new ring system derivatives, 7-substituted 2-phenyl-4H-pyridazinothiadiazin-8(7H)

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