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2H-1,4-Benzothiazine, 4-benzoyl-3,4-dihydro- is a chemical compound with the molecular formula C14H11NOS2. It belongs to the class of organic compounds known as benzothiazinones, which are characterized by a benzene ring fused to a thiazine ring. This specific compound features a benzoyl group attached to the 4-position of the benzothiazine core, and the 3,4-dihydro prefix indicates that the molecule has two hydrogen atoms added to the 3 and 4 positions, making the ring partially saturated. 2H-1,4-Benzothiazine, 4-benzoyl-3,4-dihydro- has potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other organic compounds. Its unique structure and properties make it an interesting target for further research and development.

6397-17-7

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6397-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6397-17-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6397-17:
(6*6)+(5*3)+(4*9)+(3*7)+(2*1)+(1*7)=117
117 % 10 = 7
So 6397-17-7 is a valid CAS Registry Number.

6397-17-7Relevant academic research and scientific papers

Construction of nitrogen-fused tetrahydroquinolines via a domino reaction

Gigant, Nicolas,Gillaizeau, Isabelle

supporting information, p. 4622 - 4625 (2012/10/29)

An efficient domino approach for the diastereoselective synthesis of polyfunctionalized nitrogen-fused tetrahydroquinoline frameworks under mild conditions has been developed. The scope and limitation of this transformation were investigated by using a range of readily accessible enamides and benzyl azides. This method is also applicable to the formation of 2,3-functionalized enamides.

Eliminative Ring Fission of 4-Acyl-2,3-dihydro-4H-1,4-benzothiazines

Babudri, F.,Florio, S.,Indelicati, G.,Trapani, G.

, p. 4082 - 4087 (2007/10/02)

The behavior of 4-acyl-2,3-dihydro-1,4-benzothiazines 1-11 upon treatment with lithium diisopropylamide (LDA) in THF at -78 deg C has been examined.Very marked differences have been observed.Whereas unsubstituted and monosubstituted derivatives (1-4) read

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