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189308

Sigma-Aldrich

4-Bromphenethylamin

98%

Synonym(e):

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

Lineare Formel:
BrC6H4CH2CH2NH2
CAS-Nummer:
73918-56-6
Molekulargewicht:
200.08
EG-Nummer:
277-636-2
MDL-Nummer:
MFCD00008189
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24851377
NACRES:
NA.22

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.574 (lit.)

bp

63-72 °C/0.2 mmHg (lit.)

Dichte

1.29 g/mL at 25 °C (lit.)

SMILES String

NCCc1ccc(Br)cc1

InChI

1S/C8H10BrN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2

InChIKey

ZSZCXAOQVBEPME-UHFFFAOYSA-N

Anwendung

Used in a synthesis of alkyl arylamino sufides employing elemental sulfur and a variety of halides (benzyl, allyl, primary, etc).
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.

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H314

Gefahreneinstufungen

Eye Dam. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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Sigma-Aldrich

435597

Schwefelsäure, rauchend

4-Bromphenethylalkohol 99%

Sigma-Aldrich

183431

4-Bromphenethylalkohol

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)
Boyoung Han et al.
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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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