Cas 117182-67-9,(R)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((S)-5-isopropenyl-2-methyl-cyclopent-1-enyl)-methanol

117182-67-9

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Basic information

Product Name: (R)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((S)-5-isopropenyl-2-methyl-cyclopent-1-enyl)-methanol
Synonyms:
CAS NO:117182-67-9
Molecular Formula:
Molecular Weight: 394.598
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)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((S)-5-isopropenyl-2-methyl-cyclopent-1-enyl)-methanol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((S)-5-isopropenyl-2-methyl-cyclopent-1-enyl)-methanol(117182-67-9)
EPA Substance Registry System: (R)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((S)-5-isopropenyl-2-methyl-cyclopent-1-enyl)-methanol(117182-67-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 117182-67-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117182-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,8 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117182-67:
(8*1)+(7*1)+(6*7)+(5*1)+(4*8)+(3*2)+(2*6)+(1*7)=119
119 % 10 = 9
So 117182-67-9 is a valid CAS Registry Number.

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117182-67-9Relevant academic research and scientific papers

Total Synthesis of Dictymal, a B-seco-Dictymenoid Aldehyde from an Alga, Dictyota dichotoma

Kato, Nobuo,Tanaka, Shinya,Kataoka, Hideo,Takeshita, Hitoshi

, p. 2295 - 2298 (2007/10/02)

A B-seco-dictymenoid aldehyde, dictymal, was synthesized from two optically active iridoid synthons; the required ring system was constructed by lactol-regulated Cope rearrangement and stereoselective Li-tert-BuOH-in-HMPA reduction of the tetrasubstituted

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