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75854

Sigma-Aldrich

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:
90940-54-8
Molecular Weight:
243.73
Beilstein/REAXYS Number:
8937583
MDL number:
MFCD03095466
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
57652588
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.

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)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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