Cas 1291058-19-9,4-phenyl-3,4-dihydro-1H-2,1,3-(3,4-dimethoxybenzo)thiadiazine 2,2-dioxide

1291058-19-9

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Basic information

Product Name: 4-phenyl-3,4-dihydro-1H-2,1,3-(3,4-dimethoxybenzo)thiadiazine 2,2-dioxide
Synonyms: 4-phenyl-3,4-dihydro-1H-2,1,3-(3,4-dimethoxybenzo)thiadiazine 2,2-dioxide
CAS NO:1291058-19-9
Molecular Formula:
Molecular Weight: 320.369
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-phenyl-3,4-dihydro-1H-2,1,3-(3,4-dimethoxybenzo)thiadiazine 2,2-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: 4-phenyl-3,4-dihydro-1H-2,1,3-(3,4-dimethoxybenzo)thiadiazine 2,2-dioxide(1291058-19-9)
EPA Substance Registry System: 4-phenyl-3,4-dihydro-1H-2,1,3-(3,4-dimethoxybenzo)thiadiazine 2,2-dioxide(1291058-19-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1291058-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1291058-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,1,0,5 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1291058-19:
(9*1)+(8*2)+(7*9)+(6*1)+(5*0)+(4*5)+(3*8)+(2*1)+(1*9)=149
149 % 10 = 9
So 1291058-19-9 is a valid CAS Registry Number.

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1291058-19-9Relevant academic research and scientific papers

Facile synthesis of 4-substituted 3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxides

Lee, Chai-Ho,Jin, Guo Fan,Lim, Hyun Wha,Yang, Eun Hye,Lee, Jong-Dae,Nakamura, Hiroyuki,Ban, Hyun Seung,Kang, Sang Ook

experimental part, p. 192 - 197 (2011/10/08)

A new method for the preparation of 4-substituted 3,4-dihydro-1H-2,1,3- benzothiadiazine 2,2-dioxides is described. Treatment of t-butyl N-phenylsulfamoylcarbamate derivatives (1) with different aldehydes afforded the corresponding intramolecular cyclized

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