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Merck
CN
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文件

安全信息

391751

Sigma-Aldrich

反式-4-辛烯

technical grade, ≥90%

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About This Item

线性分子式:
CH3CH2CH2CH=CHCH2CH2CH3
CAS号:
14850-23-8
分子量:
112.21
Beilstein:
1719104
EC 号:
238-913-3
MDL编号:
MFCD00009476
UNSPSC代码:
12352100
PubChem化学物质编号:
24864400
NACRES:
NA.22

等级

technical grade

质量水平

100

检测方案

≥90%

形式

liquid

折射率

n20/D 1.412 (lit.)

bp

122-123 °C (lit.)

溶解性

water: insoluble

密度

0.715 g/mL at 25 °C (lit.)

SMILES字符串

[H]\C(CCC)=C(\[H])CCC

InChI

1S/C8H16/c1-3-5-7-8-6-4-2/h7-8H,3-6H2,1-2H3/b8-7+

InChI key

IRUCBBFNLDIMIK-BQYQJAHWSA-N

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相关类别

一般描述

trans-4-Octene is an acyclic olefin. Its synthesis has been reported. Its Raman spectra has been reported. Rate constant of the gas-phase reactions of trans-4-octene with hydroxyl radicals and ozone has been investigated. Its enantiomeric epoxidation has been studied. Its isomerization into isomeric octenes has been studied.

应用

trans-4-Octene may be used in the synthesis of the following:
  • n-nonanal
  • aliphatic unsaturated polyesters
  • 4-isopropyloctane
  • diasterioisomeric 4-(difluoroiodomethyl)-5-iodooctane
  • siliranes
  • m-dioxanes

象形图

FlameHealth hazard
GHS02,GHS08

警示用语：

Danger

危险声明

H225,H304

危险分类

Asp. Tox. 1 - Flam. Liq. 2

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

分析证书(COA)

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Raman Spectra of Hydrocarbons I. 1-Octene, cis+ trans 2-Octene, trans-3-Octene, trans-4-Octene, 4-Octyne, and 1-Octyne.
Cleveland FF.
J. Chem. Phys. , 11(1), 1-6 (1943)
The Stereochemistry of the Debromination of Vicinal Dibromides by Metals1.
Schubert WM, et al.
Journal of the American Chemical Society, 74(18), 4590-4592 (1952)
Synthesis, physicochemical studies and aerobic enantioselective epoxidation of non functionalized olefins catalyzed by new Co (II) chiral salen complexes.
Kureshy RI et al.
J. Mol. Catal. A: Chem., 121(1), 25-31 (1997)
Synthesis and characterization of aliphatic unsaturated polyesters from trans-4-octene-1, 8-dioic and trans-3-hexene-1, 6-dioic acids.
Maglio G et al.
Eur. Polymer J., 15(7), 695-699 (1979)
A convenient, mild method for the cyclization of 3-and 4-arylalkanoic acids via their trifluoromethanesulfonic anhydride derivatives
Hulin B and Koreeda M.
The Journal of Organic Chemistry, 49(1), 207-209 (1984)
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