Cas 130407-83-9,(3aR,9R,9aR,9bS)-9-Hydroxy-9-methyl-2-phenyl-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione

130407-83-9

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Basic information

Product Name: (3aR,9R,9aR,9bS)-9-Hydroxy-9-methyl-2-phenyl-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione
Synonyms: (3aR,9R,9aR,9bS)-9-Hydroxy-9-methyl-2-phenyl-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione
CAS NO:130407-83-9
Molecular Formula:
Molecular Weight: 311.381
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: (3aR,9R,9aR,9bS)-9-Hydroxy-9-methyl-2-phenyl-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,9R,9aR,9bS)-9-Hydroxy-9-methyl-2-phenyl-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione(130407-83-9)
EPA Substance Registry System: (3aR,9R,9aR,9bS)-9-Hydroxy-9-methyl-2-phenyl-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione(130407-83-9)

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: 130407-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130407-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130407-83:
(8*1)+(7*3)+(6*0)+(5*4)+(4*0)+(3*7)+(2*8)+(1*3)=89
89 % 10 = 9
So 130407-83-9 is a valid CAS Registry Number.

130407-83-9Upstream product

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130407-83-9Relevant academic research and scientific papers

Effect of allylic substituents on the face selectivity of Diels-Alder reactions of semicyclic dienes

Datta,Franck,Tripathy,Quigley,Huang,Chen,Sihaed

, p. 8472 - 8478 (2007/10/02)

Vinylcyclohexenes substituted allylically on the cyclohexene ring were examined as substrates in the Diels-Alder cycloaddition. In the octalin cycloaddition products, the relative stereochemistry of the one angular hydrogen relative to that of the allylic

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