N-苄基异丙胺
N-苄基异丙胺结构式
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常用名 | N-苄基异丙胺 | 英文名 | Benzylisopropylamine |
|---|---|---|---|---|
| CAS号 | 102-97-6 | 分子量 | 149.233 | |
| 密度 | 0.9±0.1 g/cm3 | 沸点 | 200.0±0.0 °C at 760 mmHg | |
| 分子式 | C10H15N | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 87.8±0.0 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Intramolecular and intermolecular N-H...C(5)H(5)(-) hydrogen bonding in magnesocene adducts of alkylamines. Implications for chemical vapor deposition using cyclopentadienyl source compounds.
J. Am. Chem. Soc. 124(38) , 11264-5, (2002) Magnesocene adducts of alkylamines were prepared and characterized. Treatment of 3-amino-2,4-dimethylpentane, isopropylamine, tert-butylamine, benzylamine, or N-isopropylbenzylamine with magnesocene at ambient temperature in toluene afforded the amine adducts... |
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Catalytically active polymers obtained by molecular imprinting and their application in chemical reaction engineering.
Biomol. Eng. 18(1) , 1-7, (2001) Molecular imprinting is a way of creating polymers bearing artificial receptors. It allows the fabrication of highly selective plastics by polymerizing monomers in the presence of a template. This technique primarily had been developed for the generation of b... |
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One-flask transformation of secondary amines to nitrones by oxidation with hydrogen peroxide mediated by triscetylpyridinium tetrakis oxodiperoxotungsto-phosphate (PCWP). Some mechanistic considerations. Ballistreri FP, et al.
Tetrahedron 48(40) , 8677-8684, (1992)
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