推荐产品
方案
98%
表单
liquid
折射率
n20/D 1.574 (lit.)
沸点
63-72 °C/0.2 mmHg (lit.)
密度
1.29 g/mL at 25 °C (lit.)
官能团
amine
bromo
SMILES字符串
NCCc1ccc(Br)cc1
InChI
1S/C8H10BrN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2
InChI key
ZSZCXAOQVBEPME-UHFFFAOYSA-N
应用
4-Bromophenethylamine was used in the synthesis of pyrazinoisoquinoline derivatives and N-2-(4-bromophenyl)ethyl chloroacetamide. It was also used in the synthesis of alkyl arylamino sufides employing elemental sulfur and various halides.
Used in a synthesis of alkyl arylamino sufides employing elemental sulfur and a variety of halides (benzyl, allyl, primary, etc).
警示用语:
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
监管及禁止进口产品
The Journal of organic chemistry, 71(15), 5781-5784 (2006-07-15)
We have developed two simple and high yielding one-pot syntheses of alkyl aminoaryl sulfides containing a series of four-steps: in situ protection of the free amine by reaction with a Grignard reagent, halogen-lithium exchange, sulfur insertion, and a substitution reaction
Formation of pyrazinoisoquinoline ring system by the tandem amidoalkylation and N-acyliminium ion cyclization: An efficient synthesis of Praziquantel.
Tetrahedron, 54(26), 7395-7400 (1998)
Analytical and bioanalytical chemistry, 397(2), 665-675 (2010-03-20)
Based on the template of a recently introduced derivatization reagent for aldehydes, 4-(2-(trimethylammonio)ethoxy)benzeneaminium dibromide (4-APC), a new derivatization agent was designed with additional features for the analysis and screening of biomarkers of lipid peroxidation. The new derivatization reagent, 4-(2-((4-bromophenethyl)dimethylammonio)ethoxy)benzenaminium dibromide
Drug testing and analysis, 11(3), 382-391 (2018-09-07)
Target analysis using liquid chromatography-tandem mass spectrometry is applied for rapidly detecting various prohibited doping substances. Frequent modification is required as additional substances are prohibited. We developed and validated a non-target screening method requiring no further modification because it analyzes
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