Cas 124667-69-2,(1R,3S,3aR,6S,6aS)-6-Benzoyloxy-5-hydroxy-3-phenylsulfanyl-1,2,3,3a,6,6a-hexahydro-pentalene-1,4-dicarboxylic acid dimethyl ester

124667-69-2

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Basic information

Product Name: (1R,3S,3aR,6S,6aS)-6-Benzoyloxy-5-hydroxy-3-phenylsulfanyl-1,2,3,3a,6,6a-hexahydro-pentalene-1,4-dicarboxylic acid dimethyl ester
Synonyms: (1R,3S,3aR,6S,6aS)-6-Benzoyloxy-5-hydroxy-3-phenylsulfanyl-1,2,3,3a,6,6a-hexahydro-pentalene-1,4-dicarboxylic acid dimethyl ester
CAS NO:124667-69-2
Molecular Formula:
Molecular Weight: 468.527
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: (1R,3S,3aR,6S,6aS)-6-Benzoyloxy-5-hydroxy-3-phenylsulfanyl-1,2,3,3a,6,6a-hexahydro-pentalene-1,4-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3S,3aR,6S,6aS)-6-Benzoyloxy-5-hydroxy-3-phenylsulfanyl-1,2,3,3a,6,6a-hexahydro-pentalene-1,4-dicarboxylic acid dimethyl ester(124667-69-2)
EPA Substance Registry System: (1R,3S,3aR,6S,6aS)-6-Benzoyloxy-5-hydroxy-3-phenylsulfanyl-1,2,3,3a,6,6a-hexahydro-pentalene-1,4-dicarboxylic acid dimethyl ester(124667-69-2)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 124667-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124667-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,6 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124667-69:
(8*1)+(7*2)+(6*4)+(5*6)+(4*6)+(3*7)+(2*6)+(1*9)=142
142 % 10 = 2
So 124667-69-2 is a valid CAS Registry Number.

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124667-69-2Relevant academic research and scientific papers

SYNTHETIC APPLICATIONS OF MASKED O-BENZOQUINONES. A NOVEL TOTAL SYNTHESIS OF (+/-)FORSYTHIDE AGLUCONE DIMETHYL ESTER

Liao, Chun-Chen,Wei, Ching-Peng

, p. 2255 - 2256 (1989)

The title compound has been synthesized from methyl vanillate in 10 steps and in a 15percent overall yield; the Diels-Alder reaction of masked o-benzoquinone and the oxa-di-? methane rearrangement are the key reactions.

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