75854
D-Homophenylalanine ethyl ester hydrochloride
≥98.0% (HPLC)
Synonym(s):
(−)-Ethyl (R)-2-Amino-4-phenylbutyrate hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C12H17NO2 · HCl
CAS Number:
Molecular Weight:
243.73
Beilstein/REAXYS Number:
8937583
MDL number:
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
assay
≥98.0% (HPLC)
form
powder
optical activity
[α]/D -38.0±2.0°, c = 1 in H2O
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
SMILES string
Cl.CCOC(=O)[C@H](N)CCc1ccccc1
InChI
1S/C12H17NO2.ClH/c1-2-15-12(14)11(13)9-8-10-6-4-3-5-7-10;/h3-7,11H,2,8-9,13H2,1H3;1H/t11-;/m1./s1
InChI key
PTFKZMFFSIYCOV-RFVHGSKJSA-N
Application
D-Homophenylalanine ethyl ester hydrochloride may be used to synthesize (R)-2-amino-4-phenylbutan-1-ol, an intermediate for 2,6-bis[(4R)-4,5-dihydro-4-(2-phenylethyl)-2-oxazolyl]pyridine ligand.[1]
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis of Chiral Pyridine Bis (Oxazoline) Ligands for Nickel?Catalyzed Asymmetric Negishi Cross?Couplings of Secondary Allylic Chlorides with Alkylzincs: 2, 6?Bis [(4R)?4, 5?Dihydro?4?(2?Phenylethyl)?2?Oxazolyl]?Pyridine
Lou S and Fu GC
Organic Syntheses, 310-316 (2010)
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