Cas 110793-52-7,(5β,8α)-2α,2β-dimethyl-1α-<(tert-butyldimethylsilyl)oxy>-9-carbethoxytricyclo<6.3.0.0<sup>4,8</sup>>undec-9-en-6-one

110793-52-7

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Basic information

Product Name: (5β,8α)-2α,2β-dimethyl-1α-<(tert-butyldimethylsilyl)oxy>-9-carbethoxytricyclo<6.3.0.0^4,8>undec-9-en-6-one
Synonyms:
CAS NO:110793-52-7
Molecular Formula:
Molecular Weight: 392.611
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: (5β,8α)-2α,2β-dimethyl-1α-<(tert-butyldimethylsilyl)oxy>-9-carbethoxytricyclo<6.3.0.0^4,8>undec-9-en-6-one(CAS DataBase Reference)
NIST Chemistry Reference: (5β,8α)-2α,2β-dimethyl-1α-<(tert-butyldimethylsilyl)oxy>-9-carbethoxytricyclo<6.3.0.0^4,8>undec-9-en-6-one(110793-52-7)
EPA Substance Registry System: (5β,8α)-2α,2β-dimethyl-1α-<(tert-butyldimethylsilyl)oxy>-9-carbethoxytricyclo<6.3.0.0^4,8>undec-9-en-6-one(110793-52-7)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 110793-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110793-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,7,9 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 110793-52:
(8*1)+(7*1)+(6*0)+(5*7)+(4*9)+(3*3)+(2*5)+(1*2)=107
107 % 10 = 7
So 110793-52-7 is a valid CAS Registry Number.

110793-52-7Upstream product

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110793-52-7Relevant academic research and scientific papers

SYSTEM ORIENTED DESIGN OF TRIQUINANES: STEREOCONTROLLED SYNTHESIS OF PENTALENIC ACID AND PENTALENENE

Hudlicky, T.,Sinai-Zingde, G.,Natchus, M. G.,Ranu, B. C.,Papadopolous, P.

, p. 5685 - 5722 (1987)

Pentalenic acid, 5, and pentalenene, 4, and their C-9 epimers 5a and 4a, respectively, were synthesized using and cyclopentene annulation methodology.The key steps involved internal cyclopropanation of dienes 23 or cyclopropanation of enone 25

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