Cas 91158-71-3,(1S,2S)-2-((E)-6-Furan-3-yl-2-hydroxy-3-methyl-hex-3-enyl)-1,3,3-trimethyl-cyclohexanol

91158-71-3

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Basic information

Product Name: (1S,2S)-2-((E)-6-Furan-3-yl-2-hydroxy-3-methyl-hex-3-enyl)-1,3,3-trimethyl-cyclohexanol
Synonyms:
CAS NO:91158-71-3
Molecular Formula:
Molecular Weight: 320.472
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: (1S,2S)-2-((E)-6-Furan-3-yl-2-hydroxy-3-methyl-hex-3-enyl)-1,3,3-trimethyl-cyclohexanol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S)-2-((E)-6-Furan-3-yl-2-hydroxy-3-methyl-hex-3-enyl)-1,3,3-trimethyl-cyclohexanol(91158-71-3)
EPA Substance Registry System: (1S,2S)-2-((E)-6-Furan-3-yl-2-hydroxy-3-methyl-hex-3-enyl)-1,3,3-trimethyl-cyclohexanol(91158-71-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 91158-71-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91158-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,5 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91158-71:
(7*9)+(6*1)+(5*1)+(4*5)+(3*8)+(2*7)+(1*1)=133
133 % 10 = 3
So 91158-71-3 is a valid CAS Registry Number.

91158-71-3Upstream product

91178-22-2 1-Bromo-8-ketoambliol Acetate

91158-71-3Downstream Products

91158-71-3Relevant academic research and scientific papers

Metabolites of the Marine Sponge Dendrilla sp.

Sullivan, Brian,Faulkner, D. John

, p. 3204 - 3206 (1984)

The sponge Dendrilla sp. was collected from a marine lake in Palau, Western Caroline Islands.Dendrilla sp. contained the known diterpenes dehydroambliol A (1) and norrisolide (2), together with the novel metabolites 1-bromo-8-ketoambliol A acetate (3), dendrillolide A (4), dendrillolide B (5), and dendrillolide C (6).The structures of the new metabolites were determined by interpretation of spectral data, application of a biosynthetic hypothesis, and chemical interconversions.

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