Cas 82203-98-3,5,14-diacetyl-4,5,8,9-tetrahydro-2,7-diphenyl-4,8-o-benzeno-3,9-imino-3H-3,5,6-benzotriazacycloundecine

82203-98-3

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Basic information

Product Name: 5,14-diacetyl-4,5,8,9-tetrahydro-2,7-diphenyl-4,8-o-benzeno-3,9-imino-3H-3,5,6-benzotriazacycloundecine
Synonyms:
CAS NO:82203-98-3
Molecular Formula:
Molecular Weight: 524.622
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: 5,14-diacetyl-4,5,8,9-tetrahydro-2,7-diphenyl-4,8-o-benzeno-3,9-imino-3H-3,5,6-benzotriazacycloundecine(CAS DataBase Reference)
NIST Chemistry Reference: 5,14-diacetyl-4,5,8,9-tetrahydro-2,7-diphenyl-4,8-o-benzeno-3,9-imino-3H-3,5,6-benzotriazacycloundecine(82203-98-3)
EPA Substance Registry System: 5,14-diacetyl-4,5,8,9-tetrahydro-2,7-diphenyl-4,8-o-benzeno-3,9-imino-3H-3,5,6-benzotriazacycloundecine(82203-98-3)

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: 82203-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82203-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82203-98:
(7*8)+(6*2)+(5*2)+(4*0)+(3*3)+(2*9)+(1*8)=113
113 % 10 = 3
So 82203-98-3 is a valid CAS Registry Number.

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82203-98-3Relevant academic research and scientific papers

The Acylation of 5H-2,3-Benzodiazepines. Reactions of 4-Phenyl-5H-2,3-benzodiazepine with Acyl Chlorides to give N-Acylaminoisoquinolines and/or Acylated Dimers. X-Ray Molecular Structure of 5,14-Diacetyl-4,5,8,9-tetrahydro-2,7-diphenyl-4,8-o-benzeno-3,9-

Motion, Keith R.,Mundo, David P.,Sharp, John T.,Walkinshaw, Malcolm D.

, p. 2027 - 2034 (2007/10/02)

The acylation of 4-phenyl-5H-2,3-benzodiazepine (1) with acyl halides in benzene or toluene takes either or both of two reaction paths depending on the nature of the acylation reagent, the order of mixing, and the reaction temperature.One pathway leads to

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