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93301-76-9

  • Product Name:S,E)-cyclooct-2-en-1-ol
  • Molecular Weight:126.199
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Product Details

Purity:99%

Cost-effective and customizable S,E)-cyclooct-2-en-1-ol 93301-76-9 for sale

  • Molecular Formula:C8H14O
  • Molecular Weight:126.199

93301-76-9 Relevant articles

SYNTHESIS OF STRAINED CYCLOALKENE DERIVATIVES

Beccalli, Egle M.,Marchesini, Alessandro

, p. 287 - 288 (2007/10/02)

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93301-76-9 Process route

(Z)-cyclooct-2-enone
23202-10-0

(Z)-cyclooct-2-enone

(Z)-2-cycloocten-1-ol
62249-35-8

(Z)-2-cycloocten-1-ol

(+/-)-(E)-(1R,2R)-cyclo-oct-2-en-1-ol
3212-75-7,14390-23-9,31501-39-0,31821-38-2,62210-83-7,62249-35-8,93301-75-8,93301-76-9,112018-77-6,112018-78-7,130145-04-9

(+/-)-(E)-(1R,2R)-cyclo-oct-2-en-1-ol

Conditions
Conditions Yield
With lithium aluminium tetrahydride; Yield given. Multistep reaction. Yields of byproduct given; 1.) diethyl ether, irradiation, 0 deg C, 1.5 h, 2.) 0 deg C, 10 min; room temperature, 20 min;
axial-(E)-cyclooct-2-en-1-ol
93301-76-9

axial-(E)-cyclooct-2-en-1-ol

benzyl bromide
100-39-0

benzyl bromide

C<sub>12</sub>H<sub>18</sub>N<sub>2</sub>
86997-05-9

C12H18N2

benzyl alcohol
100-51-6,185532-71-2

benzyl alcohol

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 5 h / 20 - 55 °C
1.2: 96 h
2.1: chloroform / 1 h / 20 °C
With sodium hydride; In tetrahydrofuran; chloroform; mineral oil;

93301-76-9 Upstream products

  • 23202-10-0
    23202-10-0

    (Z)-cyclooct-2-enone

93301-76-9 Downstream products

  • 86997-05-9
    86997-05-9

    C12H18N2

  • 102-04-5
    102-04-5

    1,3-Diphenylpropanone

  • 100-51-6
    100-51-6

    benzyl alcohol

  • 2645443-13-4
    2645443-13-4

    (E)-cyclooct-2-en-1-yl-(4-nitrophenyl)carbonate

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