Cas 83059-08-9,(3'Z)-6-Hydroxy-3-(5'-hydroxy-3'-methyl-3'-penten-1'-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on

83059-08-9

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Basic information

Product Name: (3'Z)-6-Hydroxy-3-(5'-hydroxy-3'-methyl-3'-penten-1'-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on
Synonyms:
CAS NO:83059-08-9
Molecular Formula:
Molecular Weight: 248.322
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: (3'Z)-6-Hydroxy-3-(5'-hydroxy-3'-methyl-3'-penten-1'-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on(CAS DataBase Reference)
NIST Chemistry Reference: (3'Z)-6-Hydroxy-3-(5'-hydroxy-3'-methyl-3'-penten-1'-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on(83059-08-9)
EPA Substance Registry System: (3'Z)-6-Hydroxy-3-(5'-hydroxy-3'-methyl-3'-penten-1'-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on(83059-08-9)

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: 83059-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83059-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,5 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83059-08:
(7*8)+(6*3)+(5*0)+(4*5)+(3*9)+(2*0)+(1*8)=129
129 % 10 = 9
So 83059-08-9 is a valid CAS Registry Number.

83059-08-9Upstream product

64809-53-6 (3-Methyl-2-penten-4-yn-1-yl)-trimethylsiylaether

83059-08-9Downstream Products

83059-08-9Relevant academic research and scientific papers

Technische Verfahren zur Synthese von Carotinoiden und verwandten Verbindungen aus 6-Oxo-isophoron. V. Synthese von Astacin

Widmer, Erich,Lukac, Teodor,Bernhard, Kurt,Zell, Reinhard

, p. 671 - 683 (1982)

Starting from optically inactive astaxanthin intermediates, the highly oxygenated carotenoid astacene was synthesized in seven steps (55percent overall yield from 6-oxo-isophorone).Key features of the new approach are base- and acid-catalyzed rearrangements of acetylenic intermediates such as those described in Schemes 2, 7 and 8.

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