N-Carbobenzoxy-β-alanine

CAS: 2304-94-1

Ref. TR-C176180

Produktinformation

• Name: N-Carbobenzoxy-β-alanine
• Synonyme: 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, 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

Beschreibung

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)

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 223.23
• Formel: C₁₁H₁₃NO₄
• Farbe/Form: Neat
• InChl: InChI=1S/C11H13NO4/c13-10(14)6-7-12-11(15)16-8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,12,15)(H,13,14)
• InChI Key: InChIKey=GEVGRLPYQJTKKS-UHFFFAOYSA-N
• SMILES: O=C(O)CCNC(=O)OCc1ccccc1