C109207
1,5-环辛二烯
contains 50-150 ppm 4-tert-Butylcatechol, 99%
别名:
1,5-COD, cis-1,5-Cyclooctadiene, COD
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关于此项目
经验公式（希尔记法）:
C8H12
化学文摘社编号:
分子量:
108.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-907-1
Beilstein/REAXYS Number:
2036542
MDL number:
产品名称
1,5-环辛二烯, contains 50-150 ppm 4-tert-Butylcatechol, 99%
InChI key
VYXHVRARDIDEHS-QGTKBVGQSA-N
InChI
1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-2,7-8H,3-6H2/b2-1-,8-7-
SMILES string
C1CC=CCCC=C1
vapor pressure
25.8 mmHg ( 37.7 °C)
6.8 mmHg ( 25 °C)
assay
99%
form
liquid
autoignition temp.
431 °F
contains
50-150 ppm 4-tert-Butylcatechol as stabilizer
50-150 ppm 4-tert-Butylcatechol
refractive index
n20/D 1.493 (lit.)
bp
149-150 °C (lit.)
mp
−69 °C (lit.)
density
0.882 g/mL at 25 °C (lit.)
Quality Level
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Application
- Bis(Aluminyl)Magnesium: A Source of Nucleophilic or Radical Aluminium-Centred Reactivity.: Investigates 1,5-Cyclooctadiene′s ability to stabilize reactive intermediates in metal complexes, which is crucial for developing new pharmaceutical agents and enhancing ligand efficiency in transition metal catalysis (Griffin et al., 2024).
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
100.4 °F - closed cup
flash_point_c
38 °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
Eleonora Cavallari et al.
The journal of physical chemistry. B, 119(31), 10035-10041 (2015-07-15)
Hyperpolarization of (13)C carboxylate signals of metabolically relevant molecules, such as acetate and pyruvate, was recently obtained by means of ParaHydrogen Induced Polarization by Side Arm Hydrogenation (PHIP-SAH). This method relies on functionalization of the carboxylic acid with an unsaturated
Adrian Tlahuext-Aca et al.
Dalton transactions (Cambridge, England : 2003), 43(42), 15997-16005 (2014-09-19)
Ni(0)-catalyzed dehydrogenation of benzylic-type imines was performed to yield asymmetrical tetra-substituted imidazoles and 2-imidazolines. This was achieved with a single operational step while maintaining good selectivity and atom economy. The catalytic system shows low to moderate tolerance for fluoro-, trifluoromethyl-
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