CAS 938-97-6

DL-p-Hidroxifenilglicina

Descripción:

DL-p-Hidroxifenilglicina, con el número CAS 938-97-6, es un derivado de aminoácido caracterizado por sus componentes fenólicos y glicina. Se presenta como un polvo cristalino blanco a blanco amarillento y es soluble en agua, reflejando su naturaleza polar debido al grupo hidroxilo y al grupo amino presentes en su estructura. Este compuesto es una mezcla racémica, lo que significa que contiene tanto los enantiómeros D como L, que pueden exhibir diferentes actividades biológicas. DL-p-Hidroxifenilglicina se estudia a menudo por sus posibles aplicaciones en farmacéuticos, particularmente en el desarrollo de analgésicos y otros agentes terapéuticos. Su similitud estructural con otros aminoácidos le permite participar en diversas vías bioquímicas, lo que lo hace de interés tanto en química medicinal como en bioquímica. Además, puede servir como un bloque de construcción quiral en la síntesis orgánica. Los datos de seguridad indican que debe manejarse con cuidado, al igual que muchas sustancias químicas, para evitar posibles riesgos para la salud.

Fórmula: 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)

Clave InChI: InChIKey=LJCWONGJFPCTTL-UHFFFAOYSA-N

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

Sinónimos:

• (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

Fórmula: C₈H₉NO₃

Pureza: >95.0%(T)(HPLC)

Forma y color: White to Light yellow powder to crystal

Peso molecular: 167.16

Ref: 3B-H1853

Benzeneacetic acid, a-amino-4-hydroxy-

CAS: 938-97-6

Fórmula: C₈H₉NO₃

Pureza: 97%

Forma y color: Solid

Peso molecular: 167.1620

Ref: IN-DA00IHUW

4-Hydroxyphenylglycine

CAS: 938-97-6

4-Hydroxyphenylglycine

Fórmula: C₈H₉NO₃

Pureza: 98%

Forma y color: white to light yellow crystal to powder

Peso molecular: 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);

Fórmula: C₈H₉NO₃

Forma y color: Off White Powder

Peso molecular: 167.162

Ref: TR-H949505

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

CAS: 938-97-6

Fórmula: C₈H₉NO₃

Pureza: 97%

Forma y color: Solid

Peso molecular: 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.

Pureza: Min. 95%

Ref: 3D-FH39249