Interesting facts
Interesting Facts about 4-(2-aminoethyl)phenol
4-(2-aminoethyl)phenol, also known as an aromatic amine, is a fascinating compound with a diverse range of applications in both industrial and research settings. Here are some key points to consider:
- Versatility in Applications: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals and dyes, showcasing its significance in organic chemistry.
- Biological Activity: The amino group in its structure contributes to its potential biological activities, making it a point of interest in medicinal chemistry for drug development.
- Structure and Properties: The unique positioning of the aminoethyl group ortho to the hydroxyl group significantly influences its reactivity and interaction with other molecules.
- Research Interest: Scientists are studying its role in creating novel materials, particularly in the field of polymers, where it may enhance thermal stability and mechanical strength.
- Environmental Considerations: As with many aromatic amines, it is essential to consider the environmental impact and safety measures associated with its use due to potential toxicity.
A quote from renowned chemist Linus Pauling emphasizes the significance of understanding chemical structures: "If you want to have good ideas, you must have many ideas." This is certainly the case with 4-(2-aminoethyl)phenol, which continues to inspire innovative research and application.
In summary, 4-(2-aminoethyl)phenol is not just a simple organic compound; it's a gateway to exploring various fields of chemistry and its applications in our world.
Synonyms
tyramine
51-67-2
4-(2-Aminoethyl)phenol
p-Tyramine
4-Hydroxyphenethylamine
2-(4-Hydroxyphenyl)ethylamine
Uteramine
Tyrosamine
Tocosine
Tyramin
Systogene
Phenol, 4-(2-aminoethyl)-
4-Hydroxyphenylethylamine
p-(2-Aminoethyl)phenol
p-Hydroxyphenethylamine
Tenosin-wirkstoff
p-Hydroxyphenylethylamine
2-(p-Hydroxyphenyl)ethylamine
Phenethylamine, p-hydroxy-
p-beta-Aminoethylphenol
Phenol, p-(2-aminoethyl)-
Benzeneethanamine, 4-hydroxy-
Tyramine base
beta-Hydroxyphenylethylamine
MFCD00008193
alpha-(4-Hydroxyphenyl)-beta-aminoethane
NSC 249188
BRN 1099914
HSDB 2132
2-p-hydroxyphenylethylamine
UNII-X8ZC7V0OX3
EINECS 200-115-8
X8ZC7V0OX3
NSC-249188
4-Hydroxy-beta-phenylethylamine
DTXSID2043874
FEMA NO. 4215
beta-(4-Hydroxyphenyl)ethylamine
CHEBI:15760
p-.beta.-Aminoethylphenol
4-(2-aminoethyl)-Phenol
4 Hydroxyphenethylamine
CHEMBL11608
MLS000079096
p-Hydroxy-.beta.-phenethylamine
2-(4'-Hydroxyphenyl)ethylamine
DTXCID0023874
4-Hydroxy-.beta.-phenylethylamine
.beta.-(4-Hydroxyphenyl)ethylamine
4-13-00-01788 (Beilstein Handbook Reference)
NSC249188
NCGC00016011-08
SMR000059295
.alpha.-(4-Hydroxyphenyl)-.beta.-aminoethane
CAS-51-67-2
[3H]tyramine
[3H]-Tyramine
SR-01000075365
L-Tyramine
4-aminoethylphenol
AEF
Tyramine, free base
Tyramine (Standard)
Tyramine, 99%
Spectrum_001213
Opera_ID_887
TYRAMINE [FHFI]
TYRAMINE [HSDB]
TYRAMINE [MI]
TYRAMINE [VANDF]
Tyramine, 98%, FG
p-hydroxy-phenylethylamine
Spectrum2_000738
Spectrum3_000693
Spectrum4_001801
Spectrum5_000501
Lopac-T-2879
p-(2-aminoethyl)-Phenol
P-hydroxy-b-phenethylamine
Biomol-NT_000075
bmse000243
bmse000870
bmse000891
TYRAMINE [WHO-DD]
4-hydroxy-Benzeneethanamine
(4-hydroxyphenyl)ethylamine
cid_5610
SCHEMBL4111
WLN: Z2R DQ
4-(2-amino-ethyl)-phenol
P-hydroxy-b-phenylethylamine
4- (2-aminoethyl)-Phenol
4-Hydroxy-b-phenylethylamine
Lopac0_001136
Oprea1_294339
BSPBio_002445
KBioGR_002405
KBioSS_001693
p-Hydroxy-beta-phenethylamine
SPECTRUM210400
Tyramine, analytical standard
b-(4-Hydroxyphenyl)ethylamine
BIDD:ER0507
DivK1c_000918
2-(4-hydroxyphenyl)ethanamine
SPBio_000696
p-Hydroxy-beta-phenylethylamine
BPBio1_001394
GTPL2148
GTPL2150
SGCUT00017
2-(4-hydroxy-phenyl)ethylamine
2-(4-Hydroxyphenyl)-ethylamine
BDBM29135
HMS502N20
KBio1_000918
KBio2_001693
KBio2_004261
KBio2_006829
KBio3_001665
NINDS_000918
p-Hydroxy-.beta.-phenylethylamine
HMS1923C19
HMS2235J05
HMS3885C17
a-(4-Hydroxyphenyl)-b-aminoethane
HY-W007606R
to_000085
4-(2-Aminoethyl)-phenol(thyramin)
Tox21_110282
BBL027695
CCG-39684
MFCD00149002
s3625
STK531130
AKOS000156022
Tox21_110282_1
CS-W007606
DB08841
FT34615
HY-W007606
SDCCGSBI-0051103.P003
benzene, 1-(2-amino)ethyl-4-hydroxy-
benzene, 1-(2-aminoethyl)-4-hydroxy-
IDI1_000918
NCGC00016011-01
NCGC00016011-02
NCGC00016011-03
NCGC00016011-04
NCGC00016011-05
NCGC00016011-06
NCGC00016011-07
NCGC00016011-09
NCGC00016011-10
NCGC00016011-11
NCGC00016011-12
NCGC00016011-14
NCGC00016011-16
NCGC00016011-19
NCGC00016011-20
NCGC00063825-04
NCGC00063825-05
NCGC00063825-06
NCGC00063825-07
NCGC00063825-08
1ST40050
AS-11671
SY002127
Tyramine, Vetec(TM) reagent grade, 99%
alpha.-(4-Hydroxyphenyl)-beta-aminoethane
A0302
NS00000072
EN300-51746
C00483
AB00051887-15
Q165930
doi:10.14272/DZGWFCGJZKJUFP-UHFFFAOYSA-N.1
SR-01000075365-5
BRD-K53893978-001-03-1
Ractopamine hydrochloride suspension impurity, tyramine-
InChI=1/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H
RACTOPAMINE HYDROCHLORIDE SUSPENSION IMPURITY, TYRAMINE- [USP IMPURITY]
200-115-8
Solubility of 4-(2-aminoethyl)phenol
The solubility of 4-(2-aminoethyl)phenol (C8H11NO) can be influenced by various factors such as temperature, pH, and the presence of other solvents. As a compound that contains both an amino group and a phenolic hydroxyl group, it exhibits interesting solubility characteristics:
In summary, 4-(2-aminoethyl)phenol is expected to be relatively soluble in polar solvents, while its solubility in non-polar solvents may be limited. This interconnected blend of properties makes the study of its solubility both fascinating and complex.