2-(4-Bromophenyl)ethylamine

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2-(4-Bromophenyl)ethylamine

  • Name 2-(4-Bromophenyl)ethylamine
  • CAS 73918-56-6
  • Purity 99%
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1.What is the 2-(4-Bromophenyl)ethylamine ?

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.

4-Bromophenylacetonitrile
16532-79-9

4-Bromophenylacetonitrile

4-Bromophenethylamine
73918-56-6

4-Bromophenethylamine

Conditions
Conditions Yield
With sodium tetrahydroborate; {[κ3-(1-pz)2HB(N=CHCH3)]Ru(cymene)}+ TfO-; sodium t-butanolate; In methanol; at 70 ℃; for 14h;
85%
With methanol; sodium tetrahydroborate; C18H25BN5Ru(1+)*CF3O3S(1-); sodium t-butanolate; for 14h; Reagent/catalyst; Reflux;
85%
With samarium diiodide; water; triethylamine; In tetrahydrofuran; at 20 ℃; for 0.0833333h; Inert atmosphere;
83%
4-Bromophenylacetonitrile; With borane-THF; In tetrahydrofuran; at 0 ℃; for 24.5h; Reflux;
for 4h; Reflux;
80%
4-Bromophenylacetonitrile; With borane-THF; 5-bromoisoindoline; In tetrahydrofuran; at 75 ℃;
With hydrogenchloride; water; In tetrahydrofuran; at 20 ℃;
78%
With lithium aluminium tetrahydride; diethyl ether;
With lithium aluminium tetrahydride;
With dimethylsulfide borane complex; In tetrahydrofuran; Heating;
With borane-THF; In tetrahydrofuran; for 8h; Reflux;
1-bromo-4-ethenyl-benzene
2039-82-9

1-bromo-4-ethenyl-benzene

4-Bromophenethylamine
73918-56-6

4-Bromophenethylamine

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: NOCl, HCl / diethyl ether
2: Et3 N / diethyl ether
3: LiAlH4 / diethyl ether
With hydrogenchloride; lithium aluminium tetrahydride; nitrosylchloride; triethylamine; In diethyl ether;
With D-Glucose; ammonia; oxygen; In aq. phosphate buffer; at 30 ℃; for 24h; regioselective reaction; Green chemistry;
Multi-step reaction with 3 steps
1: oxygen; styrene monooxygenase / Enzymatic reaction
2: styrene oxide isomerase / Enzymatic reaction
3: ammonia; ω-transaminase; L-alanine dehydrogenase / Enzymatic reaction
With styrene monooxygenase; L-alanine dehydrogenase; ω-transaminase; styrene oxide isomerase; ammonia; oxygen;
With 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate; ammonium carbonate; 2-amino-benzenethiol; In dichloromethane; acetonitrile; at 20 ℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation;

2.What is the CAS number for 2-(4-Bromophenyl)ethylamine ?

The CAS number of 2-(4-Bromophenyl)ethylamine is 73918-56-6.

More information of 2-(4-Bromophenyl)ethylamine 73918-56-6 are:

CAS?Number

73918-56-6

Density

1.407 g/cm3

Boiling Point

271.3 °C at 760 mmHg

Flash Point

113.1 °C

Vapor Pressure

0.00649mmHg at 25°C

Refractive Index

n20/D 1.574(lit.)

HS CODE

29214990

PSA

26.02000

LogP

2.65060

Pka

9.72±0.10(Predicted)

3.What are another words for 2-(4-Bromophenyl)ethylamine ?

Synonyms?for?2-(4-Bromophenyl)ethylamine 73918-56-6:2-(4-Bromophenyl)ethanamine;2-(4-Bromophenyl)ethylamine;4-Bromobenzeneethanamine;4-Bromophenylethylamine;p-Bromophenethylamine;p-Bromophenylethylamine;

4.What is the molecular formula of 2-(4-Bromophenyl)ethylamine?

The chemical formula of ?2-(4-Bromophenyl)ethylamine is?C8H10BrN which containing 8 Carbon atoms,10 Hydrogen atoms,1 Bromine atoms and 1 Nitrogen atoms,and the molecular weight of??2-(4-Bromophenyl)ethylamine?is 200.078.

5.What is 2-(4-Bromophenyl)ethylamine (73918-56-6) used for?

2-(4-Bromophenyl)ethylamine is an organic compound that features a bromo substituent on a phenyl ring attached to an ethylamine group. This chemical structure endows it with unique properties that make it a versatile building block in organic synthesis and a precursor in the production of various pharmaceuticals and chemical compounds.

InChI:InChI=1/C8H10BrN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2/p+1

Relevant articles related to 2-(4-Bromophenyl)ethylamine:

Article

Source

Photocatalytic divergent decarboxylative amination: a metal-free access to aliphatic amines and hydrazines

Shu, Xianli,Xu, Ruting,Liao, Saihu

, p. 1756 - 1762 (2021/09/06)

GPR40 receptor stimulant, and preparation method, pharmaceutical composition and application thereof

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Paragraph 0163-0168; 0170, (2019/10/15)

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