CAS 14328-51-9

(αS)-α-Aminocyclohexaneacetic acid

Description:

(αS)-α-Aminocyclohexaneacetic acid, also known as L-α-amino-α-cyclohexaneacetic acid, is an amino acid derivative characterized by its cyclohexane ring structure. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), which are typical functional groups found in amino acids. The presence of the cyclohexane ring contributes to its unique steric and electronic properties, influencing its reactivity and interactions with biological systems. It is a chiral molecule, with the (αS) designation indicating the specific stereochemistry at the alpha carbon. This stereochemistry can significantly affect its biological activity and interactions with enzymes and receptors. The compound is of interest in pharmaceutical research, particularly in the development of drugs that target specific biological pathways. Its solubility in water and organic solvents can vary, impacting its formulation and application in various chemical and biological contexts. Overall, (αS)-α-Aminocyclohexaneacetic acid is a valuable compound in both synthetic and medicinal chemistry.

Formula: C₈H₁₅NO₂

InChI: InChI=1S/C8H15NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h6-7H,1-5,9H2,(H,10,11)/t7-/m0/s1

InChI key: InChIKey=WAMWSIDTKSNDCU-ZETCQYMHSA-N

SMILES: [C@H](C(O)=O)(N)C1CCCCC1

Synonyms:

• (1-Ammoniocyclohexyl)Acetate
• (2S)-2-Amino-2-cyclohexylacetic acid
• (2S)-2-Amino-2-cyclohexylethanoic acid
• (2S)-amino(cyclohexyl)ethanoic acid
• (S)-2-Amino-2-cyclohexylacetic acid
• (S)-2-Cyclohexylglycine
• (αS)-α-Aminocyclohexaneacetic acid
• <span class="text-smallcaps">L</span>-Cyclohexylglycine
• <span class="text-smallcaps">L</span>-α-Cyclohexylglycine
• Amino(Cyclohexyl)Acetic Acid
• Cyclohexaneacetic acid, α-amino-, (S)-
• Cyclohexaneacetic acid, α-amino-, (αS)-
• Cyclohexaneacetic acid, α-amino-, <span class="text-smallcaps">L</span>-
• H-Chg-OH
• L-(+)-2-Cyclohexylglycine
• L-Cyclohexyglycine
• L-Cyclohexyl glycine
• L-alpha-Cyclohexylglycine
• Cyclohexaneacetic acid, α-amino-, L-
• L-α-Cyclohexylglycine
• L-2-CYCLOHEXYLGLYCINE HYDROCHLORIDE
• L-CYCLOHEXYLGLYCINE 98%
• H-L-Chg-OH*HCl
• H-CHG-OH HCL
• L-a-cyclobenzyl glycine
• H-PHG(HEXAHYDRO)-OH HCL
• L-2-CYCLOHEXYLGLYCINE TRIFLUOROACETATE
• HEXAHYDRO-L-PHENYLGLYCINE HYDROCHLORIDE
• H-Cyclohexyl-Gly-OH (H-Chg-OH: L-2-Cyclohexylglycine)
• H-CYCLOHEXYL-GLY-OH HCL
• L-ALPHA-CYCLOHEXYLGLYCINE HYDROCHLORIDE SALT
• L-ALPHA-CYCLOHEXYLGYCINE HYDROCHLORIDE SALT
• H-CHG-OH TFA
• H-CYCLOHEXYL-GLY-OH TFA
• L-CYCLOHEXYLGLYCINE HYDROCHLORIDE
• (S)-CYCLOHEXYLGLYCINE HCL

L-2-Cyclohexylglycine

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 157.21

Ref: 3B-C2569

L-(+)-2-Cyclohexylglycine, 98%

CAS: 14328-51-9

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₈H₁₅NO₂

Purity: 98%

Color and Shape: Powder, White

Molecular weight: 157.21

Ref: 02-H26881

H-Chg-OH

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 157.2102

Ref: IN-DA003R6L

L-Cyclohexylglycine u3000

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Molecular weight: 157.22

Ref: 7W-GM3629

L-(+)-2-Cyclohexylglycine

CAS: 14328-51-9

L-(+)-2-Cyclohexylglycine

Purity: 98%

Molecular weight: 157.21g/mol

Ref: 54-OR350213

2-Cyclohexyl-L-glycine

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Purity: 97%

Color and Shape: Solid, Powder

Molecular weight: 157.213

Ref: 10-F034414

L-a-Cyclohexylglycine

CAS: 14328-51-9

L-a-Cyclohexylglycine is an efficient, general method for the preparation of peptide aldehydes. It is a serine protease inhibitor that binds to thrombin and prevents it from converting fibrinogen into fibrin. L-a-Cyclohexylglycine has been shown to inhibit polymerization of fibrinogen and factor XIII, as well as the formation of thrombin, which is important for blood clotting. L-a-Cyclohexylglycine also inhibits hepatitis C virus (HCV) replication in vitro by binding to the HCV NS3 helicase protein. This compound has been shown to be able to inhibit HIV-1 protease activity and may have potential use as an antiviral agent.

Formula: C₈H₁₅NO₂

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 157.21 g/mol

Ref: 3D-FC43992