189308
4-Bromophenethylamine
98%
Synonym(s):
2-(4-Bromophenyl)ethan-1-amine, 2-(4-Bromophenyl)ethanamine, 2-(4-Bromophenyl)ethylamine, 4-Bromobenzeneethanamine, 4-Bromophenylethylamine, p-Bromophenethylamine, p-Bromophenylethylamine
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About This Item
Linear Formula:
BrC6H4CH2CH2NH2
CAS Number:
Molecular Weight:
200.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
277-636-2
MDL number:
Assay:
98%
Form:
liquid
assay
98%
form
liquid
refractive index
n20/D 1.574 (lit.)
bp
63-72 °C/0.2 mmHg (lit.)
density
1.29 g/mL at 25 °C (lit.)
functional group
amine, bromo
SMILES string
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
Application
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).
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
监管及禁止进口产品
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Mark Eggink et al.
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
Jungyeob Ham et al.
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.
Kim JH, et al.
Tetrahedron, 54(26), 7395-7400 (1998)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 189308-1G | 04061836817558 |
| 189308-10G | 04061836817541 |
| 189308-5G | 04061836817565 |