CAS 938-97-6

DL-p-Idrossifenilglicina

Descrizione:

DL-p-Idrossifenilglicina, con il numero CAS 938-97-6, è un derivato di amminoacido caratterizzato dai suoi componenti fenolici e glicina. Esiste come una polvere cristallina bianca a bianco sporco ed è solubile in acqua, riflettendo la sua natura polare a causa del gruppo idrossile e del gruppo amminico presenti nella sua struttura. Questo composto è una miscela racemica, il che significa che contiene sia gli enantiomeri D che L, che possono mostrare diverse attività biologiche. DL-p-Idrossifenilglicina è spesso studiato per le sue potenziali applicazioni in farmacologia, in particolare nello sviluppo di analgesici e altri agenti terapeutici. La sua somiglianza strutturale con altri amminoacidi gli consente di partecipare a varie vie biochimiche, rendendolo di interesse sia in chimica medicinale che in biochimica. Inoltre, può servire come un blocco costruttivo chirale nella sintesi organica. I dati di sicurezza indicano che deve essere maneggiato con cura, come molte sostanze chimiche, per evitare potenziali rischi per la salute.

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

Sinonimi:

• (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

Purezza: >95.0%(T)(HPLC)

Colore e forma: White to Light yellow powder to crystal

Peso molecolare: 167.16

Ref: 3B-H1853

Benzeneacetic acid, a-amino-4-hydroxy-

CAS: 938-97-6

Formula: C₈H₉NO₃

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 167.1620

Ref: IN-DA00IHUW

4-Hydroxyphenylglycine

CAS: 938-97-6

4-Hydroxyphenylglycine

Formula: C₈H₉NO₃

Purezza: 98%

Colore e forma: white to light yellow crystal to powder

Peso molecolare: 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

Colore e forma: Off White Powder

Peso molecolare: 167.162

Ref: TR-H949505

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

CAS: 938-97-6

Formula: C₈H₉NO₃

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 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.

Purezza: Min. 95%

Ref: 3D-FH39249