190438

(S)-(−)-2-Amino-3-phenyl-1-propanol

98%, optical purity ee: 99% (HPLC)

• Sinonimo/i: L-Phenylalaninol
• Formula condensata: C₆H₅CH₂CH(NH₂)CH₂OH
• Numero CAS: 3182-95-4
• Peso molecolare: 151.21
• Beilstein: 2208238
• Numero CE: 221-674-4
• Numero MDL: MFCD00004732
• Codice UNSPSC: 12352116
• ID PubChem: 24851436
• NACRES: NA.22

Proprietà

• Livello qualitativo: 100
• Saggio: 98%
• Forma fisica: solid
• Attività ottica: [α]22/D −22.8°, c = 1.2 in 1 M HCl
• Purezza ottica: ee: 99% (HPLC)
• Punto di fusione: 92-94 °C (lit.)
• Stringa SMILE: N[C@H](CO)Cc1ccccc1
• InChI: 1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m0/s1; STVVMTBJNDTZBF-VIFPVBQESA-N

Descrizione

Descrizione generale

(S)-(-)-2-Amino-3-phenyl-1-propanol is a chiral amino alcohol.

Applicazioni

(S)-(-)-2-Amino-3-phenyl-1-propanol can undergo condensation with 5-nitro­salicylaldehyde to form (S)-2-[(1-benzyl-2-hydroxy­ethyl­imino)meth­yl]-4-nitro­phenol, a new chiral Schiff base. It reacts with substituted salicylaldehydes to form tridentate chiral Schiff base ligands, which can form H-bonded chiral supramolecular metal-organic architectures. It can also be used in the synthesis of an unnatural tripeptide, which can enhance the antimicrobial activity of methicillin against methicillin resistant Staphylococcus aureus.

Reacts with nitriles to form oxazolines which are useful in Pd-catalyzed allylic substitution. Also employed in amidation for chiral resolution and NADH modeling.

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 8A - Combustible corrosive hazardous materials
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Dispositivi di protezione individuale: Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges