Cas 1255768-07-0,(-)-dimethyl (3aR,8R,8aR,8bS)-1,3-dioxo-2,8-diphenyl-2,3,3a,4,6,8,8a,8b-octahydrocyclopenta[e]isoindole-7,7(1H)-dicarboxylate

1255768-07-0

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Basic information

Product Name: (-)-dimethyl (3aR,8R,8aR,8bS)-1,3-dioxo-2,8-diphenyl-2,3,3a,4,6,8,8a,8b-octahydrocyclopenta[e]isoindole-7,7(1H)-dicarboxylate
Synonyms:
CAS NO:1255768-07-0
Molecular Formula:
Molecular Weight: 459.499
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: (-)-dimethyl (3aR,8R,8aR,8bS)-1,3-dioxo-2,8-diphenyl-2,3,3a,4,6,8,8a,8b-octahydrocyclopenta[e]isoindole-7,7(1H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (-)-dimethyl (3aR,8R,8aR,8bS)-1,3-dioxo-2,8-diphenyl-2,3,3a,4,6,8,8a,8b-octahydrocyclopenta[e]isoindole-7,7(1H)-dicarboxylate(1255768-07-0)
EPA Substance Registry System: (-)-dimethyl (3aR,8R,8aR,8bS)-1,3-dioxo-2,8-diphenyl-2,3,3a,4,6,8,8a,8b-octahydrocyclopenta[e]isoindole-7,7(1H)-dicarboxylate(1255768-07-0)

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: 1255768-07-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1255768-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,7,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1255768-07:
(9*1)+(8*2)+(7*5)+(6*5)+(5*7)+(4*6)+(3*8)+(2*0)+(1*7)=180
180 % 10 = 0
So 1255768-07-0 is a valid CAS Registry Number.

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1255768-07-0Relevant academic research and scientific papers

Platinum(II) chloride-catalyzed stereoselective domino enyne isomerization/diels-alder reaction

Schelwies, Mathias,Farwick, Andreas,Rominger, Frank,Helmchen, Guenter

experimental part, p. 7917 - 7919 (2011/02/25)

Chiral 1,6-enynes were prepared via Ir-catalyzed allylic substitutions. Their platinum(II) chloride-catalyzed domino enyne isomerization/Diels-Alder reaction provided stereoselective access to complex heterocycles. Very high diastereoselectivity was induc

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