Cas 1621065-37-9,1-(2-phenylethyl)-1,2,3,4-tetrahydropyrimidino[1,2-b][1,2,4]benzothiadiazine 6,6-dioxide

1621065-37-9

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Basic information

Product Name: 1-(2-phenylethyl)-1,2,3,4-tetrahydropyrimidino[1,2-b][1,2,4]benzothiadiazine 6,6-dioxide
Synonyms: 1-(2-phenylethyl)-1,2,3,4-tetrahydropyrimidino[1,2-b][1,2,4]benzothiadiazine 6,6-dioxide
CAS NO:1621065-37-9
Molecular Formula:
Molecular Weight: 341.434
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: 1-(2-phenylethyl)-1,2,3,4-tetrahydropyrimidino[1,2-b][1,2,4]benzothiadiazine 6,6-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-phenylethyl)-1,2,3,4-tetrahydropyrimidino[1,2-b][1,2,4]benzothiadiazine 6,6-dioxide(1621065-37-9)
EPA Substance Registry System: 1-(2-phenylethyl)-1,2,3,4-tetrahydropyrimidino[1,2-b][1,2,4]benzothiadiazine 6,6-dioxide(1621065-37-9)

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: 1621065-37-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1621065-37-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,1,0,6 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1621065-37:
(9*1)+(8*6)+(7*2)+(6*1)+(5*0)+(4*6)+(3*5)+(2*3)+(1*7)=129
129 % 10 = 9
So 1621065-37-9 is a valid CAS Registry Number.

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1621065-37-9Relevant academic research and scientific papers

Unexpected heteroannulation and chlorination of benzothiadiazine derivatives mediated by DDQ

Verones, Valerie,Flouquet, Nathalie,Farce, Amaury,Berthelot, Pascal,Lebegue, Nicolas

, p. 235 - 241 (2014/03/21)

In the course of studies directed toward the synthesis of new tubulin polymerization inhibitors, several benzothiadiazine derivatives were prepared. The oxidative dehydrogenation reaction with DDQ unexpectedly led to heteroannulation and chlorination of the benzothiadiazine tricycles. A rationale for their formation is proposed.

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