CAS 15871-58-6
:(3R,4R)-4-amino-1-$l^{1}-oxidanyl-2,2,5,5-tetramethyl-pyrrolidine-3-carboxylic acid
Description:
(3R,4R)-4-amino-1-(l-oxidanyl)-2,2,5,5-tetramethyl-pyrrolidine-3-carboxylic acid, with CAS number 15871-58-6, is a chiral amino acid derivative characterized by its unique pyrrolidine ring structure. This compound features a carboxylic acid functional group, which contributes to its acidic properties, and an amino group that imparts basic characteristics, making it a zwitterionic molecule at physiological pH. The presence of multiple methyl groups on the pyrrolidine ring enhances its steric bulk, influencing its solubility and reactivity. The specific stereochemistry, indicated by the (3R,4R) configuration, plays a crucial role in its biological activity and interactions with enzymes and receptors. This compound is of interest in pharmaceutical and biochemical research, particularly in the development of peptide-based drugs and as a potential building block in organic synthesis. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, making it essential to consider these conditions in experimental applications.
Formula:C9H17N2O3
InChI:InChI=1/C9H17N2O3/c1-8(2)5(7(12)13)6(10)9(3,4)11(8)14/h5-6H,10H2,1-4H3,(H,12,13)/t5-,6+/m0/s1
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Found 4 products.
1-Pyrrolidinyloxy, 3-amino-4-carboxy-2,2,5,5-tetramethyl-, (3R,4R)-rel- (9CI)
CAS:Formula:C10H19N2O3Molecular weight:215.2695rac trans-3-Amino-1-oxyl-2,2,5,5-tetramethylpyrrolidine-4-carboxylic Acid
CAS:Controlled ProductApplications A spin-label.
References Tominaga, M., et al.: Chem. Pharm. Bull., 49, 1027 (2001), Wright, K., et al.: Tetrahedron Letters, 44, 4183 (2003)Formula:C10H19N2O3Color and Shape:NeatMolecular weight:215.27rac trans-3-amino-1-oxyl-2,2,5,5-tetramethylpyrrolidine-4-carboxylic acid
CAS:Rac-trans-3-amino-1-oxyl-2,2,5,5-tetramethylpyrrolidine 4-carboxylic acid (rac TAT) is an axial chiral compound. It has a molecular weight of 246.36 and the empirical formula C11H19N3O4. Rac TAT is soluble in water and alcohols. Rac TAT crystallizes as a racemic mixture of enantiomers (Rac=50% + 50%). Rac TAT has been used as a probe for cyclic secondary amines with high resolution. Rac TAT also shows high selectivity for β-amino acids over α-amino acids. The configuration of the molecule is determined by the configuration of the biphenyl substituents at C4 and C5. Rac TAT can be synthesized from racemic trans 3 amino 1 oxyl 2 2 5 5 tetramethyl pyrrolidin 4Formula:C9H17N2O3Purity:Min. 95%Color and Shape:PowderMolecular weight:201.24 g/mol
