Información del producto
- 3-(Benzyloxycarbonylamino)propanoic Acid
- 3-(Benzyloxycarbonylamino)propionic Acid
- 3-[N-(Benzyloxycarbonyl)amino]propionic Acid
- Carbobenzoxy-beta-alanine
- N-(Benzyloxycarbonyl)-beta-alanine
- N-CBZ-beta-alanine
- N-Carbobenzyloxy-beta-alanine
- N-[(Phenylmethoxy)carbonyl]-beta-alanine
- NSC 17161
- NSC 28943
- Ver más sinónimos
- NSC 657842
- 3-(Benzyloxycarbonylamino)propanoic acid
- 3-(Benzyloxycarbonylamino)propionic acid
- 3-(Cbz-amino)-propanoic acid
- 3-[N-(Benzyloxycarbonyl)amino]propionic acid
- Carbobenzoxy-β-alanine
- Carbobenzyloxy-beta-alanine
- Cbz-Beta-Alanine
- N-CBZ-β-alanine
- N-Carbobenzoyl-β-alanine
- N-Carbobenzyloxy-β-alanine
- N-[(Benzyloxy)carbonyl]-beta-alanine
- N-[(Phenylmethoxy)carbonyl]-β-alanine
- Z-β-Ala-OH
- beta-Alanine, N-[(phenylmethoxy)carbonyl]-
- β-Alanine, N-[(phenylmethoxy)carbonyl]-
- β-Alanine, N-carboxy-, N-benzyl ester
Applications N-Carbobenzoxy-β-alanine has been utilized for various synthesis applications including palladium-catalyzed asymmetric allylation of β-diketones, branched linker that can increase the potency of doxorubicin immunoconjugates, and diacridines that intercalate nucleic acids and inhibit DNA synthesis.
References Sawamura, M., et al.: J. Am. Chem. Soc. 114, 2586 (1997); King, H. D., et al.: Bioconjugate Chem. 10, 279 (1999); Denny, W. A., et al.: J. Med. Chem 28, 1568 (1985)
Propiedades químicas
Consulta técnica sobre: TR-C176180 N-Carbobenzoxy-β-alanine
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