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CAS 926641-28-3

:

(2R)-[(tert-butoxycarbonyl)amino](3-chlorophenyl)ethanoic acid

Description:
(2R)-[(tert-butoxycarbonyl)amino](3-chlorophenyl)ethanoic acid, with the CAS number 926641-28-3, is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound features a chiral center at the ethanoic acid moiety, which contributes to its stereochemistry. The presence of the 3-chlorophenyl group introduces a halogen substituent that can influence the compound's reactivity and biological activity. The Boc group is commonly used in peptide synthesis as a protective group, allowing for selective reactions without interfering with the amino functionality. This compound is likely to be soluble in polar organic solvents due to its polar functional groups, while its overall structure suggests potential applications in medicinal chemistry, particularly in the design of peptide-based therapeutics. Additionally, the presence of the chlorophenyl group may enhance lipophilicity, affecting its pharmacokinetic properties. Overall, this compound exemplifies the complexity and utility of modified amino acids in chemical and pharmaceutical research.
Formula:C13H16ClNO4
InChI:InChI=1/C13H16ClNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-5-4-6-9(14)7-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17)/t10-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](c1cccc(c1)Cl)C(=O)O)O
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