2-(4-Bromophenyl)ethylamine
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2-(4-Bromophenyl)ethylamine
- Name 2-(4-Bromophenyl)ethylamine
- CAS 73918-56-6
- Purity 99%
Product Details
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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.
-
-
16532-79-9
4-Bromophenylacetonitrile
-
-
73918-56-6
4-Bromophenethylamine
| 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;
|
-
-
2039-82-9
1-bromo-4-ethenyl-benzene
-
-
73918-56-6
4-Bromophenethylamine
| 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 |
- Paragraph 0163-0168; 0170, (2019/10/15) |
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