| Identification | Back Directory | [Name]
(S)-N-Boc-L-homoserine Ethyl Ester | [CAS]
147325-09-5 | [Synonyms]
(S)-N-Boc-L-homoserine Ethyl Ester
REF DUPL: N-BOC-L-HOMOSERINE METHYL ESTER
N-[(1,1-Dimethylethoxy)carbonyl]-L-homoserine Ethyl Ester
(S)-methyl 2-(tert-butoxycarbonylamino)-4-hydroxybutanoate | [Molecular Formula]
C11H21NO5 | [MDL Number]
MFCD18207790 | [MOL File]
147325-09-5.mol | [Molecular Weight]
247.29 |
| Chemical Properties | Back Directory | [Appearance]
Off-White to Pale Yellow | [Melting point ]
54-56°C | [storage temp. ]
-20°C Freezer | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
White to Pale Yellow |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White to Pale Yellow | [Uses]
Amino acid derivative useful for the treatment of Alzheimer disease. | [Uses]
Amino acid derivative useful for the treatment of Alzheimer's disease. | [Description]
(S)-N-Boc-L-homoserine ethyl ester is a synthetic intermediate in the synthesis of unsaturated caprolactams and monomer units for oxy-peptide nucleic acids from the starting material L-homoserine. | [References]
[1] JACOB M. JANEY. Raney-Co Mediated Reductive Cyclization of an α,β-Unsaturated Nitrile[J]. The Journal of Organic Chemistry, 2008, 73 8: 3212-3217. DOI: 10.1021/jo8000996
[2] MASAYASU KUWAHARA Masahiko S ? Miki Arimitsu. Synthesis of δ-amino acids with an ether linkage in the main chain and nucleobases on the side chain as monomer units for oxy-peptide nucleic acids[J]. Tetrahedron, 1999, 55 33: Pages 10067-10078. DOI: 10.1016/s0040-4020(99)00541-4 |
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Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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