CAS 22818-40-2: D-p-Hydroxyphenylglycine
Description:D-p-Hydroxyphenylglycine, with the CAS number 22818-40-2, is an amino acid derivative characterized by its phenolic and glycine components. It features a hydroxyl group (-OH) attached to the para position of the phenyl ring, which contributes to its solubility and reactivity. This compound is often studied for its potential applications in pharmaceuticals, particularly as a building block in the synthesis of various biologically active molecules. D-p-Hydroxyphenylglycine exhibits chirality, with specific stereochemical configurations influencing its biological activity. It is typically a white to off-white crystalline solid, soluble in water and organic solvents, making it versatile for various chemical reactions. The presence of both amino and carboxyl functional groups allows it to participate in typical amino acid reactions, such as peptide bond formation. Additionally, its structural features may enable interactions with biological receptors, making it of interest in medicinal chemistry and drug design. Overall, D-p-Hydroxyphenylglycine is a significant compound in both synthetic and biological chemistry contexts.
Formula:C8H9NO3
InChI:InChI=1S/C8H9NO3/c9-7(8(11)12)5-1-3-6(10)4-2-5/h1-4,7,10H,9H2,(H,11,12)/t7-/m1/s1
InChI key:InChIKey=LJCWONGJFPCTTL-SSDOTTSWSA-N
SMILES:O=C(O)C(N)C1=CC=C(O)C=C1
- Synonyms:
- (2R)-2-Amino-2-(4-hydroxyphenyl)acetic acid
- (2R)-2-Azaniumyl-2-(4-hydroxyphenyl)acetate
- (2R)-2-amino-2-phenylethanamide
- (2R)-amino(4-hydroxyphenyl)ethanoic acid
- (R)-(-)-alpha-Amino-(4-hydroxyphenyl)acetic acid
- (R)-(4-Hydroxyphenyl)glycine
- (R)-2-(4-Hydroxyphenyl)glycine
- (R)-2-Amino-2-(4-hydroxyphenyl)acetic acid
- (αR)-α-Amino-4-hydroxybenzeneacetic acid
- 2-(4-Hydroxy-phenyl)glycin D-Form
- See more synonyms
- 4-Hydroxy-<span class="text-smallcaps">D</span>-phenylglycine
- 4-Hydroxy-D-Phenylglycine
- <span class="text-smallcaps">D</span>-(-)-2-(4-Hydroxyphenyl)glycine
- <span class="text-smallcaps">D</span>-(-)-2-(p-Hydroxyphenyl)glycine
- <span class="text-smallcaps">D</span>-(-)-4-Hydroxyphenylglycine
- <span class="text-smallcaps">D</span>-(-)-Amino(4-hydroxyphenyl)acetic acid
- <span class="text-smallcaps">D</span>-(-)-p-Hydroxyphenylglycine
- <span class="text-smallcaps">D</span>-(-)-α-(4-Hydroxyphenyl)glycine
- <span class="text-smallcaps">D</span>-(-)-α-Amino-4-hydroxyphenylacetic acid
- <span class="text-smallcaps">D</span>-(-)-α-Amino-p-hydroxyphenylacetic acid
- <span class="text-smallcaps">D</span>-2-Amino-2-(p-hydroxyphenyl)acetic acid
- <span class="text-smallcaps">D</span>-α-p-Hydroxyphenylglycine
- Benzeneacetic acid, α-amino-4-hydroxy-, (R)-
- Benzeneacetic acid, α-amino-4-hydroxy-, (αR)-
- D(-)-Alpha-Parahydroxy Phenylglycine
- D(-)4-P-hydroxyphenylglycine
- D-(-)-2-(4-Hydroxyphenyl)Glycine
- D-p-hydroxyphenylglycine
- Glycine, 2-(p-hydroxyphenyl)-, <span class="text-smallcaps">D</span>-
- H-D-Phg(4-OH)-OH
- PH Dane-acid
- p-Hydroxy-(R)-phenylglycine
- p-Hydroxy-<span class="text-smallcaps">D</span>-phenylglycine
- Glycine, 2-(p-hydroxyphenyl)-, D-