Interesting facts
Interesting Facts About (2-aminophenyl)methanol
(2-aminophenyl)methanol, also known as o-aminobenzyl alcohol, is a fascinating compound with numerous applications and unique properties that intrigue chemists and researchers alike. Here's why this compound stands out:
- Dual Functional Group: This compound features both a hydroxyl group (–OH) and an amine group (–NH2), allowing it to participate in a variety of chemical reactions, making it a versatile molecule in organic synthesis.
- Synthesis Versatility: The compound can be synthesized through various methods, including reduction processes involving nitro compounds or via nucleophilic substitution reactions, providing ample opportunities for exploration in synthetic chemistry.
- Pharmaceutical Potential: Certain derivatives of (2-aminophenyl)methanol have been investigated for their bioactivity and potential use in pharmaceuticals. Their unique structure may lead to compounds with promising therapeutic effects.
- Understanding Structure-Activity Relationships: The presence of both amine and hydroxyl groups allows scientists to explore structure-activity relationships (SARs) which can lead to enhanced efficacy in drug discovery.
- Applications in Material Science: Beyond pharmaceuticals, (2-aminophenyl)methanol can be utilized in the development of polymers and other materials, highlighting its usefulness beyond traditional chemical applications.
As researchers delve deeper into the properties and applications of (2-aminophenyl)methanol, they are continually uncovering new potentials for this intriguing compound. Its ability to bridge gaps between organic synthesis and applied chemistry makes it a valuable subject for study among students and professionals alike.
Synonyms
2-Aminobenzyl alcohol
5344-90-1
(2-Aminophenyl)methanol
2-aminobenzylalcohol
2-Aminobenzenemethanol
o-Aminobenzyl alcohol
Benzenemethanol, 2-amino-
o-(Hydroxymethyl)aniline
o-Aminobenzylic alcohol
2-Hydroxymethylaniline
BENZYL ALCOHOL, o-AMINO-
NSC 1173
JK3AH3NG9C
EINECS 226-293-7
o-Aminophenylcarbinol
BRN 1072211
(o-Aminophenyl)methanol
NSC-1173
UNII-JK3AH3NG9C
DTXSID6063800
EC 226-293-7
3-13-00-01615 (Beilstein Handbook Reference)
oAminobenzyl alcohol
2Aminobenzenemethanol
oAminobenzylic alcohol
Benzyl alcohol, oamino
o(Hydroxymethyl)aniline
Benzenemethanol, 2amino
DTXCID0041436
226-293-7
inchi=1/c7h9no/c8-7-4-2-1-3-6(7)5-9/h1-4,9h,5,8h
vyfoavadnihptr-uhfffaoysa-n
(2-Amino-phenyl)-methanol
MFCD00007749
O-AMINO-BENZYLALCOHOL
(2-aminophenyl)-methanol
2-(Hydroxymethyl)aniline
1bio
o-aminobenzylalcohol
Mianserin Hydrochloride Imp. C (EP); Mianserin Imp. C (EP); (2-Aminophenyl)methanol; Benzocaine Impurity B; Mianserin Hydrochloride Impurity C; Mianserin Impurity C
2-aminophenylmethanol
0-aminobenzyl alcohol
2-amino-benzylalcohol
o-amino-benzyl alcohol
2-amino-benzenemethanol
2-amino-benzyl alcohol
WLN: ZR B1Q
Oprea1_783408
SCHEMBL16252
2-Aminobenzyl alcohol, 98%
CHEMBL1235999
NSC1173
STR03329
BBL027657
STK077953
AKOS000119677
CS-W004705
DB03058
FA64445
HY-W004705
PB47249
PS-3377
AC-11377
SY006439
DB-020514
A1000
NS00004005
EN300-21387
A829598
AC-907/25014178
Q27094019
F0001-1388
Z104495736
2-Hydroxymethyl aniline; 2-Aminobenzyl alcohol; 2-Amino-benzenemethanol
Solubility of (2-aminophenyl)methanol
(2-aminophenyl)methanol, with its unique molecular structure, exhibits intriguing solubility characteristics that are important for various applications. This compound primarily shows solubility in organic solvents due to its polar functional groups. Here are some key points to consider:
In summary, the solubility of (2-aminophenyl)methanol can be described as follows:
Understanding the solubility of this compound is crucial for its applications in pharmaceuticals, materials science, and organic synthesis.