Cas 98238-00-7,(3aS,7aR)-1-<(R)-α-methylbenzyl>-3a-<3,4-(methylenedioxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydro-4(1H)-indolone

98238-00-7

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Basic information

Product Name: (3aS,7aR)-1-<(R)-α-methylbenzyl>-3a-<3,4-(methylenedioxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydro-4(1H)-indolone
Synonyms: (3aS,7aR)-1-<(R)-α-methylbenzyl>-3a-<3,4-(methylenedioxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydro-4(1H)-indolone
CAS NO:98238-00-7
Molecular Formula:
Molecular Weight: 363.456
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: (3aS,7aR)-1-<(R)-α-methylbenzyl>-3a-<3,4-(methylenedioxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydro-4(1H)-indolone(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,7aR)-1-<(R)-α-methylbenzyl>-3a-<3,4-(methylenedioxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydro-4(1H)-indolone(98238-00-7)
EPA Substance Registry System: (3aS,7aR)-1-<(R)-α-methylbenzyl>-3a-<3,4-(methylenedioxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydro-4(1H)-indolone(98238-00-7)

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: 98238-00-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98238-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,3 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98238-00:
(7*9)+(6*8)+(5*2)+(4*3)+(3*8)+(2*0)+(1*0)=157
157 % 10 = 7
So 98238-00-7 is a valid CAS Registry Number.

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98238-00-7Relevant academic research and scientific papers

Total Synthesis of (-)-Crinine. Use of Tandem Cationic Aza-Cope Rearrangement/Mannich Cyclizations for the Synthesis of Enantiomerically Pure Amaryllidaceae Alkaloids

Overman, Larry E.,Sugai, Soji

, p. 745 - 749 (2007/10/02)

The total synthesis of enantiomerically pure (-)-crinine (1) in 10 steps and 6percent overall yield from cyclopentene oxide is reported.The key step was the rearrangement of 7 upon reaction with AgNO3 at 25 deg C to give cis-perhydroindolone 8 in 81 perce

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