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About This Item
线性分子式:
CH3CH2CH2CH=CHCH2CH2CH3
CAS号:
分子量:
112.21
Beilstein:
1719104
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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等级
technical grade
质量水平
方案
≥90%
表单
liquid
折射率
n20/D 1.412 (lit.)
沸点
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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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
警示用语：
Danger
危险声明
危险分类
Asp. Tox. 1 - Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
69.8 °F - closed cup
闪点(°C)
21 °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
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)
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)
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)
Rate constants for the gas-phase reaction of ozone with 1, 2-disubstituted alkenes.
Grosjean E and Grosjean D.
International Journal of Chemical Kinetics, 28(6), 461-466 (1996)
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)
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