33766-43-7

Basic information

• Product Name: (6E)-2,6-Dimethyl-8-acetoxy-1,6-octadiene-3-ol
• Synonyms: (6E)-2,6-Dimethyl-8-acetoxy-1,6-octadiene-3-ol;(E)-6-Hydroxy-3,7-dimethyl-2,7-octadienyl=acetate;Acetic acid (2E)-3,7-dimethyl-6-hydroxy-2,7-octadienyl ester;Acetic acid (E)-6-hydroxy-3,7-dimethyl-2,7-octadienyl ester
• CAS NO: 33766-43-7
• Molecular Formula: C₁₂H₂₀O₃
• Molecular Weight: 0
• Mol File: 33766-43-7.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (6E)-2,6-Dimethyl-8-acetoxy-1,6-octadiene-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (6E)-2,6-Dimethyl-8-acetoxy-1,6-octadiene-3-ol(33766-43-7)
• EPA Substance Registry System: (6E)-2,6-Dimethyl-8-acetoxy-1,6-octadiene-3-ol(33766-43-7)

Safety Data

• Hazardous Substances Data: 33766-43-7(Hazardous Substances Data)

Upstream product

• 37715-31-4 (E)-5-(3,3-dimethyloxiran-2-yl)-3-methylpent-2-enyl acetate 
• 1161835-74-0 C₁₂H₁₄⁽²⁾H₆O₃ 
• 37905-03-6 8-hydroxygeranyl acetate 
• 105-87-3 3,7-dimethyl-2E,6-octadien-1-yl acetate 

Downstream Products

• 87064-46-8 Toluene-4-sulfonic acid (4E,8E)-10-cyano-10-(1-ethoxy-ethoxy)-4,8-dimethyl-deca-4,8-dienyl ester 
• 87064-46-8 Toluene-4-sulfonic acid (4E,8Z)-10-cyano-10-(1-ethoxy-ethoxy)-4,8-dimethyl-deca-4,8-dienyl ester 
• 87064-54-8 Toluene-4-sulfonic acid (4E,8E)-4,8-dimethyl-10-oxo-deca-4,8-dienyl ester 
• 87064-47-9 Toluene-4-sulfonic acid (4E,8Z)-4,8-dimethyl-10-oxo-deca-4,8-dienyl ester 
• 87064-53-7 Acetic acid (2E,6E)-3,7-dimethyl-10-(toluene-4-sulfonyloxy)-deca-2,6-dienyl ester 
• 69778-94-5 (+)-11,12-epoxycembrene 

Relevant articles and documents

FURTHER 5-METHYL COUMARINS AND OTHER CONSTITUENTS FROM THE SUBTRIBE MUTISINAE

Key Word Index-Mutisia spinosa, M. retorsa; Trichocline sinuata; Brachyclados megalanthus; Compositae; chemotaxonomy; 5-methyl coumarins; monoterpenes; geraniol and linalol derivatives; C14-acetylenic compound.The investigation of four species from the subtribe Mutisiinae afforded eight new monoterpenes, seven 5-methyl coumarins, two closely related 5-methyl chromones, two coumarane derivatives, a p-hydroxy acetophenone derivative and a new C14-acetylene.The structures were elucidated by spectroscopic methods and a few chemical transformations.The chemotaxonomy of the Mutisiinae is discussed.

Selective isomerization of epoxides to allylic alcohols catalyzed by TiO2-supported gold nanoparticles

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Chemical transformation of terpenoids. VIII. Anodic oxidation of geranyl acetate

Constant-current electrolysis of geranyl acetate (2) in CH3CN-H2O afforded eight oxidation products (3-10) which were presumed to be formed through initial oxidation of the double bond at C6-C7. Based on the results of electrolysis of 2 in CH3CN-H218O we have found that the oxygen atom(s) in the products (3-10) is(are) derived from water used as the reaction medium.