Cas 95682-64-7,(R)-2-((2S,4aS,5S)-5-Hydroxy-4a-methyl-8-oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-propionic acid

95682-64-7

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Basic information

Product Name: (R)-2-((2S,4aS,5S)-5-Hydroxy-4a-methyl-8-oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-propionic acid
Synonyms:
CAS NO:95682-64-7
Molecular Formula:
Molecular Weight: 252.31
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: (R)-2-((2S,4aS,5S)-5-Hydroxy-4a-methyl-8-oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-((2S,4aS,5S)-5-Hydroxy-4a-methyl-8-oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-propionic acid(95682-64-7)
EPA Substance Registry System: (R)-2-((2S,4aS,5S)-5-Hydroxy-4a-methyl-8-oxo-2,3,4,4a,5,6,7,8-octahydro-naphthalen-2-yl)-propionic acid(95682-64-7)

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: 95682-64-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95682-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,8 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95682-64:
(7*9)+(6*5)+(5*6)+(4*8)+(3*2)+(2*6)+(1*4)=177
177 % 10 = 7
So 95682-64-7 is a valid CAS Registry Number.

95682-64-7Upstream product

83037-79-0 2S-(1,2,3,4,4a,5,6,7,8,8aα-decahydro-1α,5β-dihydroxy-4aβ-methyl-8-oxo-naphtalen-2β-yl)propionic acid methyl ester

95682-64-7Downstream Products

95682-64-7Relevant academic research and scientific papers

THE TOTAL SYNTHESIS OF 1-OXYGENATED EUDESMANOLIDES

Hijfte, Luc Van,Vandewalle, Maurits

, p. 4371 - 4382 (2007/10/02)

A route towards 1-oxygenated eudesmanolides, via a (2+2) photocycloaddition reaction for constructing the decalin framework is described.The following natural substances have been synthesized. (+/-)-dihydroreynosin (1), (+/-)-1-oxo-dihydromagnolialide (2)

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