CAS 29678-81-7

Acido (R)-2-idrossi-4-fenilbutirrico

Descrizione:

Acido (R)-2-idrossi-4-fenilbutirrico, noto anche come (R)-HPBA, è un composto chirale caratterizzato dai suoi gruppi funzionali idrossile e acido carbossilico. Presenta una struttura di acido butirrico con un gruppo fenile attaccato al quarto carbonio, contribuendo alle sue proprietà uniche. Questo composto è tipicamente un solido bianco a bianco sporco a temperatura ambiente ed è solubile in solventi polari come acqua e alcoli, grazie alla presenza dei gruppi idrossile e acido carbossilico. (R)-HPBA è di interesse nella ricerca farmaceutica, in particolare per le sue potenziali applicazioni terapeutiche, inclusi effetti antinfiammatori e analgesici. La chiralità della molecola è significativa, poiché l'enantiomero (R) può mostrare un'attività biologica diversa rispetto alla sua controparte (S). La sua sintesi spesso implica tecniche di sintesi asimmetrica per garantire la stereochimica desiderata. Inoltre, (R)-HPBA può fungere da blocco di costruzione nella sintesi organica, facilitando lo sviluppo di molecole più complesse nella chimica medicinale.

Formula: C₁₀H₁₂O₃

InChI: InChI=1/C10H12O3/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9,11H,6-7H2,(H,12,13)/t9-/m1/s1

InChI key: InChIKey=JNJCEALGCZSIGB-SECBINFHSA-N

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

Sinonimi:

• (2R)-2-hydroxy-4-phenylbutanoic acid
• (R)-2-Hydroxy-4-Phenyl Butyric Acid
• (R)-2-Hydroxy-4-phenylbutanoic Acid
• (r)-2-Hydroxy-4-phenylbutyricacid
• (αR)-α-Hydroxybenzenebutanoic acid
• <span class="text-smallcaps">D</span>-(-)-Benzyllactic acid
• Benzenebutanoic acid, α-hydroxy-, (R)-
• Benzenebutanoic acid, α-hydroxy-, (αR)-
• Butyric acid, 2-hydroxy-4-phenyl-, <span class="text-smallcaps">D</span>-(-)-
• Butyric acid, 2-hydroxy-4-phenyl-, D-(-)-
• D-(-)-Benzyllactic acid
• R(-)-2-HYDROXY-4-PHENYL-BUTYIC ACID
• (R)-HPBA
• (2R)-2-Hydroxy-4-phenylbutyric acid
• 2-hydroxy-4-phenylbutanoic acid2-hydroxy-4-phenylbutyric aci
• (R)-2-Hydroxy-4-pheylbutanoic Acid
• (R)-(-)-2-HYDROXY-4-PHENYLBUTYRIC ACID
• (R)-2-HYDROXY-4-PHENYLBUTYRIC ACID

Benzenebutanoic acid, α-hydroxy-, (αR)-

CAS: 29678-81-7

Formula: C₁₀H₁₂O₃

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 180.2005

Ref: IN-DA002Z30

(R)-(-)-2-Hydroxy-4-phenylbutyric acid

CAS: 29678-81-7

(R)-(-)-2-Hydroxy-4-phenylbutyric acid

Purezza: 98%

Peso molecolare: 180.20g/mol

Ref: 54-OR307154

(R)-2-Hydroxy-4-phenylbutyric Acid

CAS: 29678-81-7

Formula: C₁₀H₁₂O₃

Purezza: >97.0%(GC)(T)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 180.20

Ref: 3B-H1338

(R)-2-Hydroxy-4-phenylbutyric acid

CAS: 29678-81-7

Formula: C₁₀H₁₂O₃

Purezza: 98%

Colore e forma: Solid, White powder

Peso molecolare: 180.203

Ref: 10-F011769

(R)-2-Hydroxy-4-phenylbutanoic acid

CAS: 29678-81-7

(R)-2-Hydroxy-4-phenylbutanoic acid is an ester compound that is produced by the conversion of (S)-malic acid to its enantiomer. This reaction is catalyzed by a phosphoric acid esterase. The kinetic, immobilization, and transfer mechanisms have been characterized. The solubilized form of the enzyme was found to be more active than the crystalline form. Enzyme inhibitors such as hydrogen chloride and hydrochloric acid were also investigated in order to determine their effect on the reaction rate and product distribution. A structural formula for (R)-2-Hydroxy-4-phenylbutanoic acid was determined using nuclear magnetic resonance spectroscopy and mass spectrometry, revealing a dinucleotide phosphate as a possible intermediate in the synthesis pathway.

Formula: C₁₀H₁₂O₃

Purezza: Min. 95%

Peso molecolare: 180.2 g/mol

Ref: 3D-FH140634