Interesting facts
Exploring 1-Aminocycloheptanecarboxylic Acid
1-aminocycloheptanecarboxylic acid, often abbreviated as ACHC, is a fascinating compound in the field of organic chemistry. This compound holds particular interest due to its unique cycloheptane structure combined with both amino and carboxylic acid functionalities. Here are some intriguing aspects:
- Biological Significance: Compounds similar to ACHC are studied for their potential biological applications. They may act as intermediates in the synthesis of more complex molecules, including pharmaceuticals.
- Structural Variability: The cycloheptane ring provides a level of strain that can influence reactivity. Chemists are fascinated by how this strain can lead to unique chemical behavior compared to its cyclohexane counterparts.
- Research Applications: 1-aminocycloheptanecarboxylic acid is also a subject of interest in the study of amino acids and their derivatives, potentially offering insights into new protein structures or enzyme mechanisms.
- Potential Forms: The molecule can exist in various tautomeric forms, which can have significant effects on its chemical properties and reactivity.
- Synthesis Challenges: The creation of ACHC is not trivial and often requires advanced synthetic techniques, highlighting the complexities of organic synthesis in education and research.
As a budding chemist or a seasoned scientist, understanding the properties and implications of compounds like 1-aminocycloheptanecarboxylic acid opens doors to new research avenues and applications. This compound exemplifies the beauty and intricacy of organic chemistry, serving as a reminder that even less widely-known compounds can unveil exciting possibilities!
Synonyms
1-AMINOCYCLOHEPTANECARBOXYLIC ACID
6949-77-5
1-Aminocycloheptane-1-carboxylic acid
Cycloheptanecarboxylic acid, 1-amino-
NSC 22849
CB 1692
BRN 2802819
DTXSID60219717
0-14-00-00302 (Beilstein Handbook Reference)
DTXCID10142208
iinrzeipfqheap-uhfffaoysa-n
1-Amino-1-cycloheptanecarboxylic acid
MFCD01318229
8WG8XGP442
NSC-22849
1-amino-cycloheptanecarboxylic acid
1-amino-1-cycloheptane carboxylic acid
UNII-8WG8XGP442
SCHEMBL60473
1-aminocycloheptane carboxylic acid
ALBB-012431
NSC22849
1-amino-cycloheptane-carboxylic acid
BBL020458
STK137211
AKOS000177534
AB91401
1-AMINOCYCLOHEPTANECARBOXYLICACID
BS-12305
SY014105
DB-002281
CS-0122319
EN300-39474
Q27449812
Z317024840
1-Amino-1-cycloheptanecarboxylic acid, 95% (H-Ac7c-OH)
Solubility of 1-aminocycloheptanecarboxylic acid
1-aminocycloheptanecarboxylic acid, a cyclic amino acid, exhibits unique solubility characteristics due to its molecular structure. Understanding its solubility is essential in various chemical and biological contexts.
Key Factors Influencing Solubility:
In general, 1-aminocycloheptanecarboxylic acid is expected to be soluble in water, as evidenced by its structural properties. While it may not be as freely soluble as simpler amino acids, its ability to engage in hydrogen bonding compensates for the steric hindrance posed by the cycloaliphatic ring.
As a conclusion, one might say: "Solubility is a dance between polarity and molecular architecture." Therefore, 1-aminocycloheptanecarboxylic acid's solubility can be appreciated both in terms of its functional groups and its cyclic structure.