Cas 1381775-96-7,8-oxo-1,3,4a-triphenyl-3,4,4a,8-tetrahydropyrido[1,2-a]benzimidazole-9-yl selenocyanate

1381775-96-7

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Basic information

Product Name: 8-oxo-1,3,4a-triphenyl-3,4,4a,8-tetrahydropyrido[1,2-a]benzimidazole-9-yl selenocyanate
Synonyms: 8-oxo-1,3,4a-triphenyl-3,4,4a,8-tetrahydropyrido[1,2-a]benzimidazole-9-yl selenocyanate
CAS NO:1381775-96-7
Molecular Formula:
Molecular Weight: 518.476
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: 8-oxo-1,3,4a-triphenyl-3,4,4a,8-tetrahydropyrido[1,2-a]benzimidazole-9-yl selenocyanate(CAS DataBase Reference)
NIST Chemistry Reference: 8-oxo-1,3,4a-triphenyl-3,4,4a,8-tetrahydropyrido[1,2-a]benzimidazole-9-yl selenocyanate(1381775-96-7)
EPA Substance Registry System: 8-oxo-1,3,4a-triphenyl-3,4,4a,8-tetrahydropyrido[1,2-a]benzimidazole-9-yl selenocyanate(1381775-96-7)

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: 1381775-96-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1381775-96-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,1,7,7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1381775-96:
(9*1)+(8*3)+(7*8)+(6*1)+(5*7)+(4*7)+(3*5)+(2*9)+(1*6)=197
197 % 10 = 7
So 1381775-96-7 is a valid CAS Registry Number.

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1381775-96-7Relevant academic research and scientific papers

Thio-and selenocyanation reactions of quinone iminesderivatives of pyrido[1,2-a[benzimidazole

Slabko, Oleg Y.,Kachanov, Andrey V.,Kaminskii, Vladimir A.

, p. 2464 - 2470 (2012)

The thio-and selenocyanation of quinone monoimines of pyrido[1,2-a] benzimidazole series with the participation of dithiocyanogen and triselenodicyanide in mild reaction conditions results in formation of 9-or 6-thiocyano-and 9-selenocyano-derivatives in good yields.

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