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表单
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
储存分类代码
4.3 - Hazardous materials which set free flammable gases upon contact with water
WGK
WGK 3
闪点(°F)
-32.8 °F
闪点(°C)
-36 °C
法规信息
危险化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Synthesis of poly (2-substituted-1-propenylene)s from allylic arsonium ylides.
Mondiere R, et al.
Macromolecules, 38(3), 663-668 (2005)
Free-radical reaction of imine derivatives in water.
Miyabe H, et al.
The Journal of Organic Chemistry, 65(16), 5043-5047 (2000)
Hideto Miyabe et al.
Chemical & pharmaceutical bulletin, 52(1), 74-78 (2004-01-08)
Stannyl radical addition-cyclization of oxime ethers connected with olefin moieties was studied. The radical reactions proceeded effectively by the use of triethylborane as a radical initiator to provide the functionalized pyrrolidines via a carbon-carbon bond-forming process.
Ken-ichi Yamada et al.
The Journal of organic chemistry, 77(3), 1547-1553 (2012-01-03)
Triethylborane-mediated tin-free radical alkylation of N-alkoxycarbonyl-imines, such as N-Boc-, N-Cbz-, and N-Teoc-imines, proceeded smoothly at a low temperature (-78 to -20 °C) to give the corresponding adducts in high yield. Although the formation of isocyanate was the major unfavorable reaction
Masafumi Ueda
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 124(6), 311-319 (2004-06-01)
The aqueous medium radical reactions of a variety of imine derivatives such as oxime ether, oxime, hydrazone, nitrone, and N-sulfonylimine were investigated. Triethylborane-mediated intermolecular alkyl radical addition to glyoxylic oxime ether, oxime, and nitrone in water proceeded smoothly to give
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