Cas 1196791-31-7,(3S,5R)-3-[(1S,3Z)-1-hydroxy-5-(6-methoxy-2H-1,3-benzodioxol-4-yl)-4-methylpent-3-en-1-yl]-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}dihydrofuran-2(3H)-one

1196791-31-7

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Product Name: (3S,5R)-3-[(1S,3Z)-1-hydroxy-5-(6-methoxy-2H-1,3-benzodioxol-4-yl)-4-methylpent-3-en-1-yl]-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}dihydrofuran-2(3H)-one
Synonyms:
CAS NO:1196791-31-7
Molecular Formula:
Molecular Weight: 488.621
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,5R)-3-[(1S,3Z)-1-hydroxy-5-(6-methoxy-2H-1,3-benzodioxol-4-yl)-4-methylpent-3-en-1-yl]-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}dihydrofuran-2(3H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5R)-3-[(1S,3Z)-1-hydroxy-5-(6-methoxy-2H-1,3-benzodioxol-4-yl)-4-methylpent-3-en-1-yl]-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}dihydrofuran-2(3H)-one(1196791-31-7)
EPA Substance Registry System: (3S,5R)-3-[(1S,3Z)-1-hydroxy-5-(6-methoxy-2H-1,3-benzodioxol-4-yl)-4-methylpent-3-en-1-yl]-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}dihydrofuran-2(3H)-one(1196791-31-7)

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RTECS:
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Hazardous Substances Data: 1196791-31-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1196791-31-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,7,9 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1196791-31:
(9*1)+(8*1)+(7*9)+(6*6)+(5*7)+(4*9)+(3*1)+(2*3)+(1*1)=197
197 % 10 = 7
So 1196791-31-7 is a valid CAS Registry Number.

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1196791-31-7Relevant academic research and scientific papers

Studies of the asymmetric total synthesis of clavilactone D by the 'lariat' cyclization strategy

Yoshimitsu, Takehiko,Nojima, Shoji,Hashimoto, Masashi,Tsukamoto, Koji,Tanaka, Tetsuaki

, p. 2963 - 2969 (2009)

A route to the core structure of clavilactone D, a new member of the tyrosine kinase inhibitors, is reported. The route employs sequential cyclization initiated by iodo etherification followed by Friedel-Crafts cyclization to furnish a polycyclic lactone

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