06670
2-溴乙胺 氢溴酸盐
purum, ≥97.0% (AT)
别名:
2-氨基乙基溴 氢溴酸盐
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关于此项目
线性分子式:
BrCH2CH2NH2 · HBr
化学文摘社编号:
分子量:
204.89
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-924-2
Beilstein/REAXYS Number:
3607605
MDL number:
Assay:
≥97.0% (AT)
Form:
crystalline
InChI key
WJAXXWSZNSFVNG-UHFFFAOYSA-N
InChI
1S/C2H6BrN.BrH/c3-1-2-4;/h1-2,4H2;1H
SMILES string
Br.NCCBr
grade
purum
assay
≥97.0% (AT)
form
crystalline
bp
181.3 °C/979.2 hPa
Quality Level
solubility
water: soluble 84.02 g/L at 28 °C, soluble
density
0.98 g/cm3 at 28.3 °C
functional group
amine, bromo
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Application
2-溴乙胺氢溴酸盐（BEA-HBr）可用作反应物制备：
也可用作尼龙表面改性的烷基化剂，以获得伯/仲/叔胺基。
- 氨基功能化离子液体，1-胺乙基-3-甲基咪唑六氟磷酸盐（[2-aemim][PF6]）。[2-aemim][PF6]可作为芳族醛、丙二腈、乙酰乙酸乙酯发生Knoevenagel缩合反应合成4H-吡喃衍生物的催化剂。
- 通过环缩合反应合成2-(N-aryl-N-芳酰基)氨基-4,5-二氢噻唑衍生物的催化剂。
也可用作尼龙表面改性的烷基化剂，以获得伯/仲/叔胺基。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
142.9 °F - Pensky-Martens closed cup
flash_point_c
61.6 °C - Pensky-Martens closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Amino-functionalized ionic liquid as an efficient and recyclable catalyst for Knoevenagel reactions in water
Cai Y, et al.
Catalysis Letters, 109(1-2), 61-64 (2006)
Nylon surface modification. Part 1. Targeting the amide groups for selective introduction of reactive functionalities
Jia X, et al.
Polymer, 47(14), 4916-4924 (2006)
Synthesis and QSAR Studies in 2-(N-aryl-N-aroyl) amino-4, 5-dihydrothiazole Derivatives as Potential Antithrombotic Agents
Saxena AK, et al.
Bioorganic & Medicinal Chemistry, 9(8), 2025-2034 (2001)
S Garrod et al.
Magnetic resonance in medicine, 45(5), 781-790 (2001-04-27)
The metabolic consequences of xenobiotic-induced toxicity were investigated using high-resolution magic angle spinning (MAS) NMR spectroscopy of intact tissue. Renal papillary necrosis (RPN) was induced in Sprague-Dawley rats (n = 12) via a single i.p. dose of 250 mg/kg 2-bromoethanamine
Toshio Obata
Toxicology, 218(1), 75-79 (2005-11-08)
The present study was examined whether or not 2-bromoethyamine, a semicarbazide-sensitive amine oxidase (SSAO, EC; 1.4.3.6) inhibitor, would increase an active dopaminergic neurotoxin, 1-methyl-4-phenylpyridinium ion (MPP(+))-induced hydroxyl radical ((*)OH) generation in the rat striatum. Rats were anesthetized, and sodium salicylate
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