Cas 82866-60-2,(3E,6E,10E)-3,7,11,15-Tetramethyl-hexadeca-3,6,10,14-tetraen-1-ol

82866-60-2

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Basic information

Product Name: (3E,6E,10E)-3,7,11,15-Tetramethyl-hexadeca-3,6,10,14-tetraen-1-ol
Synonyms: (3E,6E,10E)-3,7,11,15-Tetramethyl-hexadeca-3,6,10,14-tetraen-1-ol
CAS NO:82866-60-2
Molecular Formula:
Molecular Weight: 290.489
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: (3E,6E,10E)-3,7,11,15-Tetramethyl-hexadeca-3,6,10,14-tetraen-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (3E,6E,10E)-3,7,11,15-Tetramethyl-hexadeca-3,6,10,14-tetraen-1-ol(82866-60-2)
EPA Substance Registry System: (3E,6E,10E)-3,7,11,15-Tetramethyl-hexadeca-3,6,10,14-tetraen-1-ol(82866-60-2)

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: 82866-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82866-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,6 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82866-60:
(7*8)+(6*2)+(5*8)+(4*6)+(3*6)+(2*6)+(1*0)=162
162 % 10 = 2
So 82866-60-2 is a valid CAS Registry Number.

82866-60-2Upstream product

82866-58-8 isopentenyl farnesyl ether

82866-60-2Downstream Products

82866-60-2Relevant academic research and scientific papers

BIOMIMETIC ENTRY TO ACYCLIC TERPENE SYNTHESIS. A NOVEL REARRANGEMENT OF ALLYL ETHER CATALYZED BY ORGANOALUMINUM REAGENTS

Yamamura, Yoshihiro,Umeyama, Kensuke,Maruoka, Keiji,Yamamoto, Hisashi

, p. 1933 - 1936 (2007/10/02)

The intramolecular prenyltransfer reaction is accomplished by the rearrangement of allyl ethers with (2,6-di-tert-butyl-4-methylphenoxy)methylaluminum trifluoromethanesulfonate.The present method provides a simple and highly efficient synthesis of lavandulol.

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