Cas 898540-38-0,(3S,4aR,4bS,6S,8R,8aR,10aR)-6-Acetoxy-4a,8a-dimethyl-1,5-dioxo-3-phenylselanylcarbonyl-dodecahydro-2-oxa-phenanthrene-8-carboxylic acid methyl ester

898540-38-0

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Basic information

Product Name: (3S,4aR,4bS,6S,8R,8aR,10aR)-6-Acetoxy-4a,8a-dimethyl-1,5-dioxo-3-phenylselanylcarbonyl-dodecahydro-2-oxa-phenanthrene-8-carboxylic acid methyl ester
Synonyms: (3S,4aR,4bS,6S,8R,8aR,10aR)-6-Acetoxy-4a,8a-dimethyl-1,5-dioxo-3-phenylselanylcarbonyl-dodecahydro-2-oxa-phenanthrene-8-carboxylic acid methyl ester
CAS NO:898540-38-0
Molecular Formula:
Molecular Weight: 549.479
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: (3S,4aR,4bS,6S,8R,8aR,10aR)-6-Acetoxy-4a,8a-dimethyl-1,5-dioxo-3-phenylselanylcarbonyl-dodecahydro-2-oxa-phenanthrene-8-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4aR,4bS,6S,8R,8aR,10aR)-6-Acetoxy-4a,8a-dimethyl-1,5-dioxo-3-phenylselanylcarbonyl-dodecahydro-2-oxa-phenanthrene-8-carboxylic acid methyl ester(898540-38-0)
EPA Substance Registry System: (3S,4aR,4bS,6S,8R,8aR,10aR)-6-Acetoxy-4a,8a-dimethyl-1,5-dioxo-3-phenylselanylcarbonyl-dodecahydro-2-oxa-phenanthrene-8-carboxylic acid methyl ester(898540-38-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 898540-38-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 898540-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,5,4 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 898540-38:
(8*8)+(7*9)+(6*8)+(5*5)+(4*4)+(3*0)+(2*3)+(1*8)=230
230 % 10 = 0
So 898540-38-0 is a valid CAS Registry Number.

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898540-38-0Relevant academic research and scientific papers

Synthetic studies of neoclerodane diterpenes from Salvia divinorum: Selective modification of the furan ring

Harding, Wayne W.,Schmidt, Matthew,Tidgewell, Kevin,Kannan, Pavitra,Holden, Kenneth G.,Dersch, Christina M.,Rothman, Richard B.,Prisinzano, Thomas E.

, p. 3170 - 3174 (2006)

A synthetic sequence has been developed to selectively functionalize the furan ring of the natural product salvinorin A (2a). The synthetic routes described convert the furan ring in 2a into an N-sulfonylpyrrole, oxazole or an oxadiazole. In addition, a p

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