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质量水平
方案
99%
表单
crystals
mp
170-175 °C (lit.)
SMILES字符串
Br.NCCBr
InChI
1S/C2H6BrN.BrH/c3-1-2-4;/h1-2,4H2;1H
InChI key
WJAXXWSZNSFVNG-UHFFFAOYSA-N
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应用
2-溴乙胺氢溴酸盐可作为反应物用于合成：
- 噻唑类和噻嗪类，通过硫代酰胺/卤代胺串联 S-烷基化-环脱氨基作用合成。
- 有光学活性的叔磷，通过氢氧化铯催化仲膦的 P-烷基化反应
- 仲胺，通过CsOH促进伯胺、二胺和多胺的化学选择性单-N-烷基化反应。
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 3
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
142.9 °F - Pensky-Martens closed cup
闪点(°C)
61.6 °C - Pensky-Martens closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Synthesis, 1040-1040 (2006)
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To aid in evaluating the performance of biomarkers, we measured kidney injury biomarkers in rat models of drug-induced acute kidney injury. Rats were treated with site-specific nephrotoxins, puromycin, gentamicin, cisplatin, or 2-bromoethylamine. Fifteen biomarkers (β-2-microglobulin, calbindin, clusterin, cystatin-C, KIM-1, GST-α
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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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