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Chemical structure of H-p-Carboxy-Phe-OH

GA22775

H-p-Carboxy-Phe-OH

Also known as 4-[(2S)-2-amino-2-carboxyethyl]benzoic acid

This substituted phenylalanine combines features of the acidic residues, aspartic acid and glutamic acid, and the aromatic residues, phenylalanine and tyrosine· Thus, this amino acid allows ionic, hydrogen bonding or aromatic interactions between peptidic ligands and their receptors

ChemicalCAS126109-42-0MW209.2FormulaC10H11NO4
CAS number
126109-42-0
Molecular weight
209.2
Formula
C10H11NO4
Solubility
Soluble in DMSO
InChIKey
YXDGRBPZVQPESQ-QMMMGPOBSA-N
Catalogue number
GA22775
Brand
GLPBIO
Computed properties PubChem CID 1501862 · XLogP -1.6 · TPSA 101 Ų · H-bond donors 3
XLogP
-1.6
TPSA
101 Ų
H-bond donors
3
H-bond acceptors
5
Rotatable bonds
4
Heavy atoms
15

SMILES C1=CC(=CC=C1C[C@@H](C(=O)O)N)C(=O)O

Computed descriptors from PubChem (CID 1501862), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
Ships from the manufacturer to your lab in 8–14 business days; customs and cold chain handled by LABO Scientific.
Pricing
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Documents
Lot certificate of analysis and manufacturer SDS are emailed with your order confirmation.
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