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Merck
CN

136964

Sigma-Aldrich

N-异丙基苄胺

97%

别名:

N-苄基异丙胺

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About This Item

线性分子式:
C6H5CH2NHCH(CH3)2
CAS号:
分子量:
149.23
Beilstein:
2638437
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

表单

liquid

折射率

n20/D 1.502 (lit.)

沸点

200 °C (lit.)

密度

0.892 g/mL at 25 °C (lit.)

官能团

amine
phenyl

SMILES字符串

CC(C)NCc1ccccc1

InChI

1S/C10H15N/c1-9(2)11-8-10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3

InChI key

LYBKPDDZTNUNNM-UHFFFAOYSA-N

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一般描述

N-甲基丙基苄胺在环境温度下在甲苯中与茂金属形成胺加合物

应用

N - 异丙基苄胺用作配体,用于制备和表征(环戊二烯基)镁。它也用于合成N-亚苄基异丙胺-N-氧化物

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

161.6 °F - closed cup

闪点(°C)

72 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

Lot/Batch Number

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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)
Aibing Xia et al.
Journal of the American Chemical Society, 124(38), 11264-11265 (2002-09-19)
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 Cp2Mg(NH2CH(CH(CH3)2)2) (91%), Cp2Mg(NH2iPr) (80%), Cp2Mg(NH2tBu) (67%), Cp2Mg(NH2CH2Ph) (80%), and Cp2Mg(NH(CH(CH3)2)(CH2C6H5)) (91%). These adducts
O Brüggemann
Biomolecular engineering, 18(1), 1-7 (2001-06-29)
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 biomimetic materials

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