Cas 1360110-87-7,(3R,3aR,4R,10cR)-tert-butyl 4-(4-chlorobenzoyl)-3-(4-chlorophenyl)-3-hydroxy-2-oxo-1,3,3a,4,5,10c-hexahydrocyclopenta[c]carbazole-6(2H)-carboxylate

1360110-87-7

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Basic information

Product Name: (3R,3aR,4R,10cR)-tert-butyl 4-(4-chlorobenzoyl)-3-(4-chlorophenyl)-3-hydroxy-2-oxo-1,3,3a,4,5,10c-hexahydrocyclopenta[c]carbazole-6(2H)-carboxylate
Synonyms: (3R,3aR,4R,10cR)-tert-butyl 4-(4-chlorobenzoyl)-3-(4-chlorophenyl)-3-hydroxy-2-oxo-1,3,3a,4,5,10c-hexahydrocyclopenta[c]carbazole-6(2H)-carboxylate
CAS NO:1360110-87-7
Molecular Formula:
Molecular Weight: 590.503
EINECS: N/A
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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: (3R,3aR,4R,10cR)-tert-butyl 4-(4-chlorobenzoyl)-3-(4-chlorophenyl)-3-hydroxy-2-oxo-1,3,3a,4,5,10c-hexahydrocyclopenta[c]carbazole-6(2H)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3R,3aR,4R,10cR)-tert-butyl 4-(4-chlorobenzoyl)-3-(4-chlorophenyl)-3-hydroxy-2-oxo-1,3,3a,4,5,10c-hexahydrocyclopenta[c]carbazole-6(2H)-carboxylate(1360110-87-7)
EPA Substance Registry System: (3R,3aR,4R,10cR)-tert-butyl 4-(4-chlorobenzoyl)-3-(4-chlorophenyl)-3-hydroxy-2-oxo-1,3,3a,4,5,10c-hexahydrocyclopenta[c]carbazole-6(2H)-carboxylate(1360110-87-7)

Safety Data

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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1360110-87-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360110-87-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,1,1 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1360110-87:
(9*1)+(8*3)+(7*6)+(6*0)+(5*1)+(4*1)+(3*0)+(2*8)+(1*7)=107
107 % 10 = 7
So 1360110-87-7 is a valid CAS Registry Number.

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1360110-87-7Relevant academic research and scientific papers

Multicatalytic asymmetric synthesis of complex tetrahydrocarbazoles via a Diels-Alder/benzoin reaction sequence

Liu, Yankai,Nappi, Manuel,Escudero-Adan, Eduardo C.,Melchiorre, Paolo

experimental part, p. 1310 - 1313 (2012/04/23)

Expanding upon the recently developed aminocatalytic asymmetric indole-2,3-quinodimethane strategy, a straightforward synthesis of structurally and stereochemically complex tetrahydrocarbazoles has been devised. The chemistry's complexity-generating power was further harnessed by designing a multicatalytic, one-pot Diels-Alder/benzoin reaction sequence to stereoselectively access trans-fused tetracyclic indole-based compounds having four stereogenic centers with very high fidelity.

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