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2-benzyl-5-phenyl-3-methyl-1,2,6-thiadiazine 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79991-35-8

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79991-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79991-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,9 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79991-35:
(7*7)+(6*9)+(5*9)+(4*9)+(3*1)+(2*3)+(1*5)=198
198 % 10 = 8
So 79991-35-8 is a valid CAS Registry Number.

79991-35-8Downstream Products

79991-35-8Relevant academic research and scientific papers

An improved synthesis of 2H-1,2,6-thiadiazine 1,1-dioxides by condensation of β-amino and β-chloro α,β-unsaturated ketones with sulfamides

Alberola,Andres,Gonzalez,Pedrosa,Vicente

, p. 355 - 356 (2007/10/02)

Symmetrically substituted β-amino α,β-unsaturated ketones react with sulfamide giving 2H-1,2,6-thiadiazine 1,1-dioxides in excellent yields. Unsymmetrically substituted β-amino and β-chloro α,β-unsaturated ketones also react with benzylsulfamide to yield

Synthesis and Physicochemical Properties of 1,2,6-Thiadiazine 1,1-Dioxides. A Comparative Study with Pyrazoles

Elguero, Jose,Ochoa, Carmen,Stud, Manfred,Esteban-Calderon, Carmen,Martinez-Ripoll, Martin,et al.

, p. 536 - 544 (2007/10/02)

The chemical and structural properties of 18 1,2,6-thiadiazine 1,1-dioxides have been studied.By comparison with the corresponding pyrazoles it could be established that there are some analogies between pyrazoles and thiadiazine 1,1-dioxides, but because of the great difference in aromaticity, both series of heterocycles behave quite differently in other cases.However, a rough parallelism is observed in the tautomeric equilibrium, the 13C chemical shifts, and the reactivity of the 4-position.As a consequence, the hypothesis will be made that these similarities are general and could be extended to a whole variety of heterocyclic and alicyclic structures.

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