391751
反式-4-辛烯
technical grade, ≥90%
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关于此项目
线性分子式:
CH3CH2CH2CH=CHCH2CH2CH3
化学文摘社编号:
分子量:
112.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
238-913-3
Beilstein/REAXYS Number:
1719104
MDL number:
Assay:
≥90%
Form:
liquid
InChI key
IRUCBBFNLDIMIK-BQYQJAHWSA-N
InChI
1S/C8H16/c1-3-5-7-8-6-4-2/h7-8H,3-6H2,1-2H3/b8-7+
SMILES string
[H]\C(CCC)=C(\[H])CCC
grade
technical grade
assay
≥90%
form
liquid
Quality Level
refractive index
n20/D 1.412 (lit.)
bp
122-123 °C (lit.)
solubility
water: insoluble
density
0.715 g/mL at 25 °C (lit.)
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General description
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.
Application
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
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
69.8 °F - closed cup
flash_point_c
21 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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)
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)
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)
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