Skip to main content

1-aminocyclohexanecarboxylic acid

ADVERTISEMENT
Identification
Molecular formula
C7H13NO2
CAS number
2026-50-6
IUPAC name
1-aminocyclohexanecarboxylic acid
State
State

At room temperature, 1-aminocyclohexanecarboxylic acid is a solid. It can exist in the form of crystalline powders making it slightly less dense than water.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
298.90
Boiling point (Kelvin)
572.05
General information
Molecular weight
143.19g/mol
Molar mass
143.1970g/mol
Density
1.1220g/cm3
Appearence

1-Aminocyclohexanecarboxylic acid typically appears as a white crystalline solid. The crystals are often small and may be somewhat powdery in texture depending on the method of crystallization used. It is generally odorless or may have a faint amine-like smell.

Comment on solubility

Solubility of 1-aminocyclohexanecarboxylic acid (C7H13NO2)

1-aminocyclohexanecarboxylic acid exhibits a notable solubility profile that is influenced by its molecular structure and functional groups. Here are some key points regarding its solubility:

  • Polar Nature: The presence of both an amino group (-NH2) and a carboxylic acid group (-COOH) indicates that this compound is polar, which enhances its solubility in polar solvents.
  • Solubility in Water: 1-aminocyclohexanecarboxylic acid is soluble in water due to hydrogen bonding interactions between the compound and water molecules, allowing it to dissolve effectively.
  • Solubility in Organic Solvents: In contrast, it has limited solubility in non-polar organic solvents, as the non-polar components of these solvents do not interact favorably with the polar functional groups of the compound.
  • Temperature Dependence: Like many compounds, its solubility can vary with temperature; typically, higher temperatures can increase solubility in water due to greater kinetic energy disrupting interactions in the solid state.

As a result, understanding the solubility of 1-aminocyclohexanecarboxylic acid is crucial for its applications in biological systems and chemical synthesis where solvent choice can significantly impact reactivity and stability. Overall, its solubility behaviors highlight the importance of functional groups in determining the interactions between chemical compounds and solvents.

Interesting facts

Interesting Facts about 1-Aminocyclohexanecarboxylic Acid

1-Aminocyclohexanecarboxylic acid, commonly referred to as ACHA, is a fascinating compound with several notable features that appeal to both scientists and chemistry students alike. Here are some of the interesting aspects of ACHA:

  • Structural Variety: As a cyclohexane derivative, ACHA showcases a unique cyclic structure that is characteristic of many amino acids. Its cyclic nature can affect its reactivity and biological properties.
  • Chirality: ACHA possesses a chiral center, which means it can exist in two enantiomeric forms. This chirality plays a critical role in biological systems, influencing interactions with enzymes and receptors.
  • Potential Applications: This compound is investigated for various applications in the pharmaceutical industry. Its ability to mimic natural amino acids opens up opportunities in drug design and synthesis.
  • Role in Biochemistry: 1-Aminocyclohexanecarboxylic acid is sometimes studied in the context of amino acid metabolism. Understanding its pathways could lead to insights into amino acid biosynthesis.

In terms of synthesis, ACHA can be derived through several chemical reactions, often involving the functionalization of cyclohexane derivatives. Researchers frequently explore new synthetic routes to improve yields and reduce environmental impact. As a student of chemistry, appreciating the complexity and utility of such compounds can deepen your understanding of organic reactions and materials.

Overall, 1-aminocyclohexanecarboxylic acid presents a perfect blend of structural uniqueness and potential for practical applications, making it a compound worth exploring further in both academic and industrial research.

Synonyms
1-Aminocyclohexanecarboxylic acid
2756-85-6
Homocycloleucine
1-Amino-1-cyclohexanecarboxylic acid
1-Aminocyclohexane-1-carboxylic acid
Cyclohexanecarboxylic acid, 1-amino-
alpha-Aminocyclohexanecarboxylic acid
MFCD00001487
1-Amino-1-cyclohexane carboxylic acid
.alpha.-Aminocyclohexanecarboxylic acid
NSC 9059
alpha-Aminocyclohexanecarboxylic aicd
EINECS 220-411-0
CB 1641
BRN 2355692
1SE3HD391H
1-aminocyclohexane carboxylic acid
NSC-9059
DTXSID6062626
CHEBI:86534
3-14-00-00845 (Beilstein Handbook Reference)
.alpha.-Aminocyclohexanecarboxylic aicd
H-AC6C-OH
UNII-1SE3HD391H
1-amino-cyclohexanecarboxylic acid
AC1NOMHH
Lopac-A-162
bmse000728
A819121
Lopac0_000117
SCHEMBL59793
aminocyclohexanecarboxylic acid
CHEMBL559934
1-Aminocyclohexanecarboxyic acid
DTXCID1037692
1-Amino-cyclohexanecarboxylicacid
1-Amino-cyclohexylcarboxylic acid
NSC9059
1-ammonio-1-cyclohexanecarboxylate
HMS1789H14
1-Amino-1-cyclohexanecarboxylicacid
ALBB-035214
l-aminocyclohexane-1-carboxylic acid
2-aminocyclohexane-2-carboxylic acid
BBL001486
STK133208
ZINC00116197
1-azanylcyclohexane-1-carboxylic acid
1-amino-1-cyclohexane-carboxylic acid
AKOS000119400
AC-2699
BS-3813
CCG-204212
CS-W016418
SDCCGSBI-0050105.P002
1-Aminocyclohexanecarboxylic acid, 98%
NCGC00015011-01
NCGC00015011-02
NCGC00015011-03
NCGC00015011-04
NCGC00162066-01
PD034464
SY002600
A1068
NS00014645
EN300-17792
Q27159221
F3095-1803
220-411-0