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形式
liquid
质量水平
反应适用性
reagent type: reductant
浓度
1.0 M in hexanes
密度
0.675 g/mL at 25 °C
SMILES字符串
CCB(CC)CC
InChI
1S/C6H15B/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChI key
LALRXNPLTWZJIJ-UHFFFAOYSA-N
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应用
三乙基硼烷可用于:
- 在水介质中作为自由基反应的自由基引发剂和终止剂。(1)
- 通过与2-取代的烯丙基胂叶立德反应合成聚(2-取代-1-亚丙烯基)聚合物。(2)
作为催化剂用于:
N -杂环卡宾硼烷还原烷基溴的反应物
具有氧化电位的四甲基铵三烷基苯硼酸酯盐合成用反应物
- 醛的烯丙基化
- 脱羧酶 C-C 键断裂反应
- 氢化铼/硼路易斯酸共催化烯烃加氢反应
- 不饱和肟醚的区域选择性羟基烷基化
N -杂环卡宾硼烷还原烷基溴的反应物
具有氧化电位的四甲基铵三烷基苯硼酸酯盐合成用反应物
警示用语:
Danger
危险分类
Aquatic Chronic 2 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Repr. 2 - Skin Corr. 1A - STOT RE 1 Inhalation - STOT SE 3
靶器官
Central nervous system, Nervous system
WGK
WGK 3
闪点(°F)
-32.8 °F
闪点(°C)
-36 °C
法规信息
危险化学品
Free-radical reaction of imine derivatives in water.
The Journal of Organic Chemistry, 65(16), 5043-5047 (2000)
Synthesis of poly (2-substituted-1-propenylene)s from allylic arsonium ylides.
Macromolecules, 38(3), 663-668 (2005)
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 120(8), 667-676 (2000-08-18)
Triethylborane has the potential to induce radical reactions on solid support and the solid-phase radical reactions were achieved by using triethylborane as a radical initiator. The intermolecular carbon radical addition to glyoxylic oxime ether anchored to Wang resin proceeded under
Chemical & pharmaceutical bulletin, 52(7), 842-847 (2004-07-17)
Tandem radical addition-cyclization of oxime ethers anchored to polymer support was studied. The reaction of oxime ethers with stannyl radical proceeded effectively by the use of triethylborane as a radical initiator. The alkyl radical addition-cyclization reactions of oxime ether connected
Magnetic resonance in chemistry : MRC, 44(8), 807-812 (2006-05-27)
The structures of the components in the triethylborane-mediated radical addition reaction of oxime ether were investigated by 1H- and 3D-DOSY NMR methods. It has been impossible to physically separate the unstable intermediates; therefore, the structures were thus far unidentified. It
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