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(S)-(−)-2-Amino-3-phenyl-1-propanol

ALDRICH/190438 - 98%, optical purity ee: 99% (HPLC)

Synonym: L-Phenylalaninol

CAS Number: 3182-95-4
Empirical Formula (Hill Notation): C9H13NO
Molecular Weight: 151.21
EC Number: 221-674-4
MDL Number: MFCD00004732
Linear Formula: C6H5CH2CH(NH2)CH2OH
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-190438-1G 1 g
$42.50
1/EA
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45-190438-10G 10 g
$121.00
1/EA
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assay 98%
form solid
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
InChI key STVVMTBJNDTZBF-VIFPVBQESA-N
mp 92-94 °C (lit.)
optical activity [α]22/D −22.8°, c = 1.2 in 1 M HCl
optical purity ee: 99% (HPLC)
Quality Level 100 
SMILES string N[C@H](CO)Cc1ccccc1
Application: (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.
Application: Reacts with nitriles to form oxazolines which are useful in Pd-catalyzed allylic substitution. Also employed in amidation for chiral resolution and NADH modeling.
General description: (S)-(-)-2-Amino-3-phenyl-1-propanol is a chiral amino alcohol.
Packaging: 1, 10 g in glass bottle
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3259PSN1 8 / PGIII
WGK Germany WGK 3
Purity 98%
mp 92-94 °C (lit.)
UNSPSC 12352116

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