Interesting facts
Interesting Facts about 2-Acetamido-4-methyl-pentanoic Acid
2-Acetamido-4-methyl-pentanoic acid is a fascinating compound with intriguing properties and applications. Here are some noteworthy aspects:
- Biochemical Relevance: This compound is closely related to amino acids, serving as a potential building block for various peptides and proteins. Its unique structure allows for diverse biological activity.
- Potential Therapeutic Uses: Research indicates that derivatives of this compound may exhibit beneficial effects in treating metabolic disorders and neurological conditions. These therapeutic potentials are still under investigation but are promising.
- Synthesis and Derivatives: The synthesis of 2-acetamido-4-methyl-pentanoic acid can be achieved through several organic reaction pathways, often utilizing amino acids as starting materials. This makes it an interesting subject for organic chemists.
- Chirality: Like many amino acids, this compound exhibits chiral characteristics that complicate its synthesis and influence its biological interactions. Understanding its stereochemistry is crucial for developing effective drug formulations.
- Utility in Research: Chemists often utilize this compound to investigate enzyme mechanisms and metabolic pathways, providing deeper insights into biochemical processes.
In conclusion, 2-acetamido-4-methyl-pentanoic acid embodies a unique intersection of organic chemistry, biochemistry, and potential pharmaceutical development. Its study continues to unravel new discoveries that may contribute significantly to various scientific fields.
Synonyms
N-Acetyl-DL-leucine
Acetylleucine
99-15-0
Ac-DL-Leu-OH
2-acetamido-4-methylpentanoic acid
Tanganil
Acetileucina
Acetyl-DL-leucine
Acetylleucinum
Acetylleucine [INN]
N-Acetyl-D,L-leucine
(R,S)-N-Acetylleucin
Acetylleucine, dl-
Acetileucina [Spanish]
Acetylleucinum [Latin]
DL-Leucine, N-acetyl-
NSC-122020
UNII-K76S41V71X
Acetylleucine (INN)
L-Leucine, N-acetyl-
K76S41V71X
EINECS 202-734-9
MFCD00026498
ACETYLLEUCINE [MI]
NSC-758152
RP 7452
Leucine, N-acetyl-, DL-
ACETYLLEUCINE [MART.]
ACETYLLEUCINE [WHO-DD]
DTXSID40859594
NSC 122020
NSC 758152
Acetylleucinum (Latin)
ACETYLLEUCINE (MART.)
SR-01000391875
NSC-206316
Acetyl DL-leucine
N-Acetylleucine #
Tanganil (TN)
N-Acethy-D-leucine
Oprea1_806534
MLS002207045
SCHEMBL282371
CHEMBL1875805
DTXCID00209990
N07CA04
CHEBI:166830
HMS1607L21
HY-B1442
BBL012196
NSC122020
NSC203436
NSC206311
NSC206316
STK803086
AKOS000132161
AKOS016039425
CS-4647
DB13226
FA48956
FD20065
NSC-203436
NSC-206311
AC-24095
AS-14331
SMR001306703
SY008073
SY013106
SY062212
DB-041428
DB-044961
DB-057761
A0097
EU-0067605
NS00126509
D07350
EN300-297596
M03064
Q2823840
SR-01000391875-1
SR-01000391875-2
SR-01000391875-3
Z56755951
Ac-DL-Leu-OH;(RS)-Ac-2-amino-4-methyl-pentanoic acid
F0777-0821
Solubility of 2-acetamido-4-methyl-pentanoic acid (C8H15NO3)
The solubility of 2-acetamido-4-methyl-pentanoic acid can be quite significant in various solvent systems, particularly those that feature polar characteristics. This is primarily due to the presence of functional groups within the compound that can engage in hydrogen bonding, highlighting its **potential for solvation**.
Key factors influencing solubility:
In summary, solutions of 2-acetamido-4-methyl-pentanoic acid will be more prominent in polar solvents, demonstrating ample solubility due to its **functional group interactions** and **structural characteristics**. As is often the case with many organic acids, factors such as pH and solvent polarity can significantly alter solubility profiles.