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A. Amino acids and their derivatives
A-a) Aromatic amino acids
A-b) Aliphatic amino acids
A-c) Synthons for chiral amino acids
B. Chiral carboxylic acids and their derivatives
B-a) α-Hydroxycarboxylic acids
B-b) β-Hydroxycarboxylic acids
B-c) Others
C. Chiral alcohols and their derivatives
C-a) Diols
C-b) Epoxides
C-c) Others
D. Cyclic amines and their derivatives
D-a) 3-Aminopyrrolidines
D-b) Other pyrrolidines
D-c) Piperidines
E. Intermediates for various enzyme inhibitors
E-a) For ACE inhibitors
E-b) For HMG CoA reductase inhibitors
E-c) For various protease inhibitors
F. Intermediates for penems & carbapenems
G. Peptide coupling reagents and others
G-a) Coupling reagents for peptide synthesis
G-b) Reagents for active ester method
G-c) Others
E: Intermediates for various enzyme inhibitors
E-c) For various protease inhibitors
1. [1(S)-Benzyl-2(S),3-epoxypropyl]-carbamic acid tert-butyl ester
[1(S)-Benzyl-2(S),3-epoxypropyl]-carbamic acid tert-butyl ester C15H21NO3
Mw: 263.34
CAS: [98737-29-2]
2. [1(S)-Benzyl-2(R),3-epoxypropyl]-carbamic acid tert-butyl ester
[1(S)-Benzyl-2(R),3-epoxypropyl]-carbamic acid tert-butyl ester C15H21NO3
Mw: 263.34
CAS: [98760-08-8]
3. [1(S)-Methyl-2(S),3-epoxypropyl]-carbamic acid tert-butyl ester
[1(S)-Methyl-2(S),3-epoxypropyl]-carbamic acid tert-butyl ester C9H17NO3
Mw: 187.24
CAS: [165683-88-5]
4. (2S,3S)-3-N-tert-Butoxycarbonylamino-2-hydroxy-4-phenylbutanoic acid
(2S,3S)-3-N-tert-Butoxycarbonylamino-2-hydroxy-4-phenylbutanoic acid C15H21NO5
Mw: 295.33
CAS: [116661-86-0]
5. (2S,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid
(2S,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid C10H13NO3
Mw: 195.21
CAS: [62023-62-5]
6. (2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid
(2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid C10H13NO3
Mw: 195.21
CAS: [76647-67-1]
CAS Registry Number® is a Registered Trademark of the American Chemical Society.
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