Cas 80787-71-9,8,9-dimethoxy-13-methyl-11,12,13,13a-tetrahydro[1,3]dioxolo[6,7]indeno[2,1-a][3]benzazepine

80787-71-9

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Basic information

Product Name: 8,9-dimethoxy-13-methyl-11,12,13,13a-tetrahydro[1,3]dioxolo[6,7]indeno[2,1-a][3]benzazepine
Synonyms:
CAS NO:80787-71-9
Molecular Formula:
Molecular Weight: 351.402
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: 8,9-dimethoxy-13-methyl-11,12,13,13a-tetrahydro[1,3]dioxolo[6,7]indeno[2,1-a][3]benzazepine(CAS DataBase Reference)
NIST Chemistry Reference: 8,9-dimethoxy-13-methyl-11,12,13,13a-tetrahydro[1,3]dioxolo[6,7]indeno[2,1-a][3]benzazepine(80787-71-9)
EPA Substance Registry System: 8,9-dimethoxy-13-methyl-11,12,13,13a-tetrahydro[1,3]dioxolo[6,7]indeno[2,1-a][3]benzazepine(80787-71-9)

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: 80787-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80787-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,8 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80787-71:
(7*8)+(6*0)+(5*7)+(4*8)+(3*7)+(2*7)+(1*1)=159
159 % 10 = 9
So 80787-71-9 is a valid CAS Registry Number.

80787-71-9Upstream product

1141487-14-0 8,9-dimethoxy-13-methyl-12,13-dihydro[1,3]dioxolo[6,7]indeno[2,1-a][3]benzazepin-6(11H)-one

80787-71-9Downstream Products

96681-78-6 bulgaramine

80787-71-9Relevant academic research and scientific papers

Facile synthesis of a benzindenoazepine alkaloid, bulgaramine, via samarium diiodide promoted ring expansion of an α-aminocarbonyl compound

Honda, Toshio,Aranishi, Eriko,Kaneda, Kyosuke

supporting information; experimental part, p. 1857 - 1859 (2009/09/06)

A novel synthetic path to a benzindenoazepine alkaloid was established by employing a samarium diiodide promoted ring expansion reaction of an α-amlnocarbonyl compound as a key reaction, In which a regloselectlve carbon-nitrogen bond cleavage followed by

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