Interesting facts
Interesting Facts about 2-amino-3-benzyloxy-propanoic acid
2-amino-3-benzyloxy-propanoic acid, often abbreviated as ABPA, is a fascinating compound that plays a significant role in organic chemistry. Here are some intriguing points about this compound:
- Structure: This molecule features a unique arrangement of functional groups, which includes an amino group, a propanoic acid moiety, and a benzyloxy substitution. This combination contributes to its reactivity and applications in various chemical processes.
- Biological Significance: ABPA is a derivative of amino acids and shares structural similarities with key neurotransmitters, highlighting its potential role in biological systems and pharmaceutical development.
- Applications in Synthesis: The benzyloxy group attached to the propanoic acid backbone can facilitate various reactions, making ABPA an important intermediate in the synthesis of complex organic molecules.
- Research Interest: Scientists are exploring ABPA's properties for various therapeutic applications, particularly in the field of drug development, owing to its structural versatility.
- Chirality: ABPA presents an interesting case of chirality, which is the property of a molecule to exist in two enantiomorphic forms. This feature is crucial in drug design as the different isomers can exhibit vastly different biological activities.
As noted by chemists, “The interplay between structure and function remains a cornerstone of understanding in organic chemistry.” This sentiment rings particularly true for compounds like 2-amino-3-benzyloxy-propanoic acid, as their unique characteristics lead to innovations in science and industry.
Synonyms
O-Benzyl-DL-serine
5445-44-3
H-DL-Ser(Bzl)-OH
2-amino-3-(benzyloxy)propanoic acid
2-amino-3-phenylmethoxypropanoic acid
Serine, O-(phenylmethyl)
o-Benzylserine
MFCD00021724
32520-12-0
3-Benzyloxy-DL-alanine
(R)-2-Amino-3-(benzyloxy)propanoic acid
Serine, O-(phenylmethyl)-
o-benzyl-serine
Benzyl-DL-serine
NINDS_000814
EINECS 226-650-7
Spectrum2_001351
DivK1c_000814
SCHEMBL561330
SPBio_001561
CHEMBL3039403
HMS502I16
KBio1_000814
CHEBI:181104
IDGQXGPQOGUGIX-UHFFFAOYSA-N
ALBB-025900
BCP21779
NSC22028
CCG-39289
NSC 22028
NSC-22028
AKOS006228762
IDI1_000814
AS-19069
O-Benzyl-DL-serine, >=99.0% (NT)
SY034124
SY034131
DB-011737
DB-051438
DB-321312
O-BenZyl-DL-serine (H-DL-Ser(BZl)-OH)
B0860
CS-0127982
EN300-71544
A26753
I11103
BRD-A67259561-001-02-6
H-Ser(Bzl)-OH pound>>(S)-2-Amino-3-(benzyloxy)propanoic acid
3-Hydroxy-l-phenylalanine;H-S-META-TYR-OH;H-M-TYR-OH;L-3-Hydroxy-phenylalanine
Solubility of 2-amino-3-benzyloxy-propanoic acid
2-amino-3-benzyloxy-propanoic acid, with the chemical formula C10H13NO3, exhibits characteristics that can influence its solubility in various solvents. Generally, the solubility of organic compounds is affected by factors such as polarity, molecular size, and the presence of functional groups.
In the case of 2-amino-3-benzyloxy-propanoic acid, the following points highlight its solubility features:
In summary, while 2-amino-3-benzyloxy-propanoic acid is expected to be soluble in polar solvents due to its functional groups, its solubility may be influenced by the balance of hydrophobic and hydrophilic characteristics brought forth by its unique molecular structure. As the rule of thumb states, "like dissolves like," and this compound certainly reflects that principle through its varied solubility behavior.