1,5-dimethylhex-4-enyl acetate

  • Name: 1,5-dimethylhex-4-enyl acetate
  • CAS: 19162-00-6
  • Purity: 99%
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1.What is the 1,5-dimethylhex-4-enyl acetate ?

Clear, colorless liquid; fruity aroma.

1,5-Dimethylhex-4-enyl acetate, also known as sulcatol acetate, is the acetylated derivative of sulcatol (6-methyl-5-hepten-2-ol), a pheromone involved in insect aggregation. 1,5-dimethylhex-4-enyl acetate is structurally characterized by a six-carbon chain with a double bond at the 4-position and methyl groups at the 1- and 5-positions, esterified with an acetate group. Its synthesis and enantiomeric forms have been explored, particularly in the context of pheromone research, where deracemization strategies such as Mitsunobu inversions and enzymatic resolutions are employed to obtain enantiopure forms. The acetate derivative is likely used in similar applications as the parent alcohol, such as pest control or behavioral studies in insects.

2.What is the CAS number for 1,5-dimethylhex-4-enyl acetate ?

The CAS number of 1,5-dimethylhex-4-enyl acetate is 19162-00-6.

3.What are another words for 1,5-dimethylhex-4-enyl acetate ?

Synonyms?for?1,5-dimethylhex-4-enyl acetate 19162-00-6:5-Hepten-2-ol,6-methyl-, acetate (7CI,8CI,9CI); (?à)-Sulcatol acetate; 6-Methyl-5-hepten-2-yl acetate; Sulcatol acetate

4.What is 1,5-dimethylhex-4-enyl acetate (19162-00-6) used for?

InChI:InChI=1/C10H18O2/c1-8(2)6-5-7-9(3)12-10(4)11/h6,9H,5,7H2,1-4H3

Relevant articles related to 1,5-dimethylhex-4-enyl acetate:

Article

Source

High-speed microwave-promoted Mitsunobu inversions. Application toward the deracemization of sulcatol

Steinreiber, Andreas,Stadler, Alexander,Mayer, Sandra F,Faber, Kurt,Kappe

, p. 6283 - 6286 (2001)

Essential oil of aristolochia trilobata: Synthesis, routes of exposure, acute toxicity, binary mixtures and behavioral effects on leaf-cutting ants

De Oliveira, Bruna Maria S.,Melo, Carlisson R.,Alves, Péricles B.,Santos, Abra?o A.,Santos, Ane Caroline C.,Santana, Alisson Da S.,Araújo, Ana Paula A.,Nascimento, Pedro E. S.,Blank, Arie F.,Bacci, Leandro

, (2017/03/11)

Enantioselective enzymatic resolution of racemic alcohols by lipases in green organic solvents

Belafriekh, Abderahmane,Secundo, Francesco,Serra, Stefano,Djeghaba, Zeineddine

, p. 473 - 478 (2017/03/23)

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