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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 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)
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)
Addition of dimesitylsilylene to olefins. A reinvestigation.
Zhang S, et al.
Journal of the American Chemical Society, 113(11), 4278-4281 (1991)
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)
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