(+)-(1S,3R)-3-Amino-cyclopentane carboxylic acid

CAS : 71830-07-4

Ref. 3D-FA56210

Informations sur le produit

• Nom: (+)-(1S,3R)-3-Amino-cyclopentane carboxylic acid
• Synonymes: (+)-(1S,3R)-b-Homocycloleucine, (+)-(1R,3S)-1-amino-cyclopent-2-ene-4-carboxylic acid, (+)-cis-3-Aminocyclopentanecarboxylic acid, (1S,3R)-3-Aminocyclopentane-1-carboxylic acid, Cyclopentanecarboxylic acid, 3-amino-, (1S,3R)-, Cyclopentanecarboxylic acid, 3-amino-, (1S-cis)-, L-AcPAC, (+)-(1S,3R)-3-Aminocyclopentanecarboxylic acid, (1S,3R)-3-Aminocyclopentanecarboxylic acid

Description

The nature of the amino acid side chain plays a major role in determining the properties of an amino acid. The side chain is either hydrophobic (CH3) or hydrophilic (NH2). Amino acids are arranged into subunits. The alpha-amino group is attached to the carbon atom at the end of the side chain, and the carboxyl group is attached to a second carbon atom on a different molecule. These two molecules are joined by a chemical bond called an amide bond. The alpha-carboxyl group determines whether an amino acid will be acidic or basic in nature. The pH scale ranges from 0 to 14, with 7 being neutral, and numbers higher than 7 indicating alkaline conditions. Constant values for each amino acid can be found on this website:

The exciplex is formed when two molecules emit light of different wavelength that combine and produce one wavelength of light. Kinetics refers to the rates at which reactions occur, while diastere

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 129.16 g/mol
• Formule: C₆H₁₁NO₂
• Degré de pureté: Min. 95%
• Couleur/Forme: White Powder
• InChI: InChI=1S/C6H11NO2/c7-5-2-1-4(3-5)6(8)9/h4-5H,1-3,7H2,(H,8,9)/t4-,5+/m0/s1
• Code InChI: InChIKey=MLLSSTJTARJLHK-CRCLSJGQSA-N
• SMILES: N[C@@H]1CC[C@H](C(=O)O)C1