Cas 160715-33-3,(4S,4aS,7S,8R,8aS)-4-((S)-4-Benzyloxy-3-methyl-butyryl)-8-hydroxy-7-isopropyl-4a-methyl-octahydro-naphthalen-2-one

160715-33-3

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Basic information

Product Name: (4S,4aS,7S,8R,8aS)-4-((S)-4-Benzyloxy-3-methyl-butyryl)-8-hydroxy-7-isopropyl-4a-methyl-octahydro-naphthalen-2-one
Synonyms: (4S,4aS,7S,8R,8aS)-4-((S)-4-Benzyloxy-3-methyl-butyryl)-8-hydroxy-7-isopropyl-4a-methyl-octahydro-naphthalen-2-one
CAS NO:160715-33-3
Molecular Formula:
Molecular Weight: 414.585
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: (4S,4aS,7S,8R,8aS)-4-((S)-4-Benzyloxy-3-methyl-butyryl)-8-hydroxy-7-isopropyl-4a-methyl-octahydro-naphthalen-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,4aS,7S,8R,8aS)-4-((S)-4-Benzyloxy-3-methyl-butyryl)-8-hydroxy-7-isopropyl-4a-methyl-octahydro-naphthalen-2-one(160715-33-3)
EPA Substance Registry System: (4S,4aS,7S,8R,8aS)-4-((S)-4-Benzyloxy-3-methyl-butyryl)-8-hydroxy-7-isopropyl-4a-methyl-octahydro-naphthalen-2-one(160715-33-3)

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: 160715-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160715-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,7,1 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 160715-33:
(8*1)+(7*6)+(6*0)+(5*7)+(4*1)+(3*5)+(2*3)+(1*3)=113
113 % 10 = 3
So 160715-33-3 is a valid CAS Registry Number.

160715-33-3Upstream product

160715-33-3Downstream Products

215227-89-7 (S)-4-Benzyloxy-1-((1R,3S,4S,7S,8R,9S)-7-isopropyl-1-methoxy-4-methyl-11-oxa-tricyclo[6.2.1.0^4,9]undec-3-yl)-3-methyl-butan-1-one

160715-33-3Relevant academic research and scientific papers

Approach to the Synthesis of Enantiomerically Pure Chatancin. I. Synthesis of (1R,2S,6S,7R,8S,3'S)-2-(4'-Benzyloxy-3'-methylbutoyl)-7-hydroxy-8-isopropyl-1-methylbicyclodecan-4-on

Aichberger, W. D.,Aigner, J.,Goessinger, E.,Gruber, K.,Menz, G.

, p. 991 - 1010 (2007/10/02)

Our first target on the way towards the synthesis of enantiomerically pure chatancin is the preparation of the title compound.The cycloadduct of 5,5-dimethoxy-1,2,3,4-tetrachlorocyclopentadiene and thymoquinone is stereo- and regioselectively reduced to t

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