Cas 84574-63-0,2,2a,2b,7,7a,7b-hexahydro-7-oxo-N-phenyl-1H-benzo<f>cycloprop<cd>indene-1,2-dicarboximide

84574-63-0

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Basic information

Product Name: 2,2a,2b,7,7a,7b-hexahydro-7-oxo-N-phenyl-1H-benzocyclopropindene-1,2-dicarboximide
Synonyms:
CAS NO:84574-63-0
Molecular Formula:
Molecular Weight: 329.355
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: 2,2a,2b,7,7a,7b-hexahydro-7-oxo-N-phenyl-1H-benzocyclopropindene-1,2-dicarboximide(CAS DataBase Reference)
NIST Chemistry Reference: 2,2a,2b,7,7a,7b-hexahydro-7-oxo-N-phenyl-1H-benzocyclopropindene-1,2-dicarboximide(84574-63-0)
EPA Substance Registry System: 2,2a,2b,7,7a,7b-hexahydro-7-oxo-N-phenyl-1H-benzocyclopropindene-1,2-dicarboximide(84574-63-0)

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: 84574-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 84574-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84574-63:
(7*8)+(6*4)+(5*5)+(4*7)+(3*4)+(2*6)+(1*3)=160
160 % 10 = 0
So 84574-63-0 is a valid CAS Registry Number.

84574-63-0Upstream product

84574-57-2 5,8-endo-etheno-5,6,7,8-tetrahydro-9-oxo-N-phenylbenzocyclohepten-6,7-dicarboximide

84574-63-0Downstream Products

84574-63-0Relevant academic research and scientific papers

PHOTOCHEMISTRY OF ETHENOBENZOCYCLOHEPTENONES. A DI-?-METHANE REARRANGEMENT OF β,γ-UNSATURATED ARYL KETONES

Hassner, Alfred,Middlemiss, David,Murray-Rust, Judith,Murray-Rust, Peter

, p. 2539 - 2546 (1982)

Benzotropones 6 react with dienophiles 7 to give endo-adducts 8 as shown by PMR.Unlike similar ketones which usually undergo 1,3-acyl shifts or oxadi-?-methane rearrangements, these ethenobenzocycloheptenones 8, on direct or sensitized irradiation, lead t

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