CAS 938-97-6

DL-p-Hydroxyphenylglycine

Description:

DL-p-Hydroxyphenylglycine, with the CAS number 938-97-6, is an amino acid derivative characterized by its phenolic and glycine components. It exists as a white to off-white crystalline powder and is soluble in water, reflecting its polar nature due to the hydroxyl group and the amino group present in its structure. This compound is a racemic mixture, meaning it contains both the D- and L-enantiomers, which can exhibit different biological activities. DL-p-Hydroxyphenylglycine is often studied for its potential applications in pharmaceuticals, particularly in the development of analgesics and other therapeutic agents. Its structural similarity to other amino acids allows it to participate in various biochemical pathways, making it of interest in both medicinal chemistry and biochemistry. Additionally, it may serve as a chiral building block in organic synthesis. Safety data indicates that it should be handled with care, as with many chemical substances, to avoid potential health hazards.

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)

InChI key: InChIKey=LJCWONGJFPCTTL-UHFFFAOYSA-N

SMILES: C(C(O)=O)(N)C1=CC=C(O)C=C1

Synonyms:

• (2S)-ammonio(4-hydroxycyclohexyl)ethanoate
• (4-Hydroxyphenyl)glycine
• (RS)-2-(4-Hydroxyphenyl)glycine
• (±)-2-(p-Hydroxyphenyl)glycine
• (±)-Amino(p-hydroxyphenyl)acetic acid
• (±)-p-Hydroxyphenylglycine
• (±)-α-Amino-4-hydroxybenzeneacetic acid
• 2-(4-Hydroxyphenyl)glycine
• 2-Amino-2-(4-hydroxyphenyl)acetic acid
• 2-Amino-2-(4-hydroxyphenyl)aceticacid
• <span class="text-smallcaps">DL</span>-2-(4-Hydroxyphenyl)glycine
• <span class="text-smallcaps">DL</span>-2-(p-Hydroxyphenyl)glycine
• <span class="text-smallcaps">DL</span>-4-Hydroxyphenylglycine
• <span class="text-smallcaps">DL</span>-p-Hydroxyphenylglycine
• <span class="text-smallcaps">DL</span>-α-Amino(4-hydroxyphenyl)acetic acid
• Benzeneacetic acid, α-amino-4-hydroxy-
• DL-Para-Hydroxyphenylglycine
• DL-p-Hydroxyphenylglycine
• Dl-4-Hydroxyphenylglycine
• Glycine, 2-(p-hydroxyphenyl)-
• NSC 30081
• p-Hydroxy Phenylglycine
• α-(4-Hydroxyphenyl)glycine
• α-(p-Hydroxyphenyl)glycine
• α-Amino-4-hydroxyphenylacetic acid

DL-2-(4-Hydroxyphenyl)glycine

CAS: 938-97-6

Formula: C₈H₉NO₃

Purity: >95.0%(T)(HPLC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 167.16

Ref: 3B-H1853

Benzeneacetic acid, a-amino-4-hydroxy-

CAS: 938-97-6

Formula: C₈H₉NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 167.1620

Ref: IN-DA00IHUW

4-Hydroxyphenylglycine

CAS: 938-97-6

4-Hydroxyphenylglycine

Formula: C₈H₉NO₃

Purity: 98%

Color and Shape: white to light yellow crystal to powder

Molecular weight: 167.16g/mol

Ref: 54-OR12450

(4-Hydroxyphenyl)glycine

CAS: 938-97-6

Applications (4-Hydroxyphenyl)glycine, is a key intermediate for the synthesis Cefpiramide (C243400), used as a β-lactam antibiotic.
References Xiao, R. Q., et al.: Guangzhou Huagong, 41, 111 (2013);

Formula: C₈H₉NO₃

Color and Shape: Off White Powder

Molecular weight: 167.162

Ref: TR-H949505

2-Amino-2-(4-hydroxyphenyl)acetic acid

CAS: 938-97-6

Formula: C₈H₉NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 167.164

Ref: 10-F236720

DL-4-Hydroxyphenylglycine

CAS: 938-97-6

DL-4-Hydroxyphenylglycine is an active analogue of the natural amino acid L-glycine, which is a precursor in the biosynthesis of sulfamides. DL-4-Hydroxyphenylglycine has been shown to be active as an anti-infective agent against many bacteria and fungi that are resistant to other sulfa drugs. It is synthesized by reacting sodium carbonate and ammonia with the amide of 4-hydroxybenzeneacetic acid. The cyclic peptide is then hydrolyzed to form free DL-4-hydroxyphenylglycine. This drug has also been shown to have a strong inhibitory effect on fatty acid metabolism in liver cells, which may be due to its ability to bind to fatty acids and reduce their uptake by cells.

Purity: Min. 95%

Ref: 3D-FH39249