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2H-Pyrido[4,3-e]-1,2,4-thiadiazine, 2-methyl-1,1-dioxide (9CI) is a chemical compound with the molecular formula C6H5N3O2S. It belongs to the class of pyridothiadiazine derivatives, which are heterocyclic compounds containing a pyridine ring fused with a thiadiazine ring. This specific compound features a methyl group at the 2-position and a dioxide group at the 1,1-position. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential anti-inflammatory, analgesic, and antipyretic properties. The compound's structure and properties make it a valuable building block in the development of new therapeutic agents and chemical research.

164406-90-0

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164406-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164406-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,4,0 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 164406-90:
(8*1)+(7*6)+(6*4)+(5*4)+(4*0)+(3*6)+(2*9)+(1*0)=130
130 % 10 = 0
So 164406-90-0 is a valid CAS Registry Number.

164406-90-0Downstream Products

164406-90-0Relevant academic research and scientific papers

Synthesis and structural studies of a new class of heterocyclic compounds: 1,2,4-Pyridothiadiazine 1,1-dioxides, pyridyl analogues of 1,2,4-benzothiadiazine 1,1-dioxides

De Tullio, Pascal,Pirotte, Bernard,Dupont, Leon,Masereel, Bernard,Laeckmann, Didier,Podona, Tchao,Diouf, Ousmane,Lebrun, Philippe,Delarge, Jacques

, p. 3221 - 3234 (1995)

A series of novel 1,2,4-pyridothiadiazine 1,1-dioxides (1), some of them being pyridyl analogues of the 1,2,4-benzothiadiazine 1,1-dioxide diazoxide (2), were synthesized and selected physicochemical data (pKa, log P′) were collected. By means of spectral (13C NMR, UV) and X-ray data, the most favourable position of the C=N double bond in the thiadiazine ring was discussed. It was concluded that like 1,2,4-benzothiadiazine 1,1-dioxides, 1,2,4-pyridothiadiazine 1,1-dioxides free of an alkyl substituent in the 2-and 4-positions, whatever the nitrogen atom position in the pyridine ring, show predominance of the tautomeric 4H-form.

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