N-Cbz-L-aspartic Acid

CAS: 1152-61-0

Rif. TR-C176285

Informazioni sul prodotto

• Nome: N-Cbz-L-aspartic Acid
• Sinonimi: N-[(Phenylmethoxy)carbonyl]-L-aspartic Acid, N-Carboxy-L-aspartic Acid N-Benzyl Ester, Benzyloxycarbonyl-L-aspartic Acid, Carbobenzoxy-L-aspartic Acid, Cbz-Asp-OH, N-(Benzyloxycarbonyl)-L-aspartic Acid, N-Benzyloxylcarbonyl-L-aspartic Acid, N-Carbobenzoxy-L-aspartic Acid, N-Carbobenzyloxy-L-aspartic Acid, NSC 88479, NSC 9972, (2S)-2-(Phenylmethoxycarbonylamino)butanedioic acid, (2S)-2-[[(Benzyloxy)carbonyl]amino]butanedioic acid, (2S)-2-{[(benzyloxy)carbonyl]amino}butanedioate, <span class="text-smallcaps">L</span>-Aspartic acid, N-[(phenylmethoxy)carbonyl]-, Aspartic acid, N-carboxy-, N-benzyl ester, Aspartic acid, N-carboxy-, N-benzyl ester, <span class="text-smallcaps">L</span>-, Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-aspartic acid, CBZ-L-Aspartic Acid-OH, Carbobenzoxy-<span class="text-smallcaps">L</span>-aspartic acid, Cbz-L-aspartic acid, N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-aspartic acid, N-Benzyloxycarbonyl-L-aspartic acid, N-Benzyloxylcarbonyl-<span class="text-smallcaps">L</span>-aspartic acid, N-CBZ-L-Aspartic acid N-Carbobenzyloxy-L-aspartic acid, N-Carbobenzoxy-<span class="text-smallcaps">L</span>-aspartic acid, N-Carbobenzoxy-L-aspatic acid, N-Carbobenzyloxy-<span class="text-smallcaps">L</span>-aspartic acid, N-Cbz-L-Asp-OH, N-Cbz-L-aspartic acid, N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-aspartic acid, N-[(benzyloxy)carbonyl]-D-aspartic acid, N-[(benzyloxy)carbonyl]-L-aspartic acid, N-[(benzyloxy)carbonyl]aspartic acid, N-cbz-L-aspartic acid crystalline, NALPHA-Benzyloxycarbonyl-L-aspartic acid, Z-Asp-OH, Z-L-Aspartic acid, z-Asp
• CAS: 1152-61-0

Descrizione

Applications N-Cbz-L-aspartic acid is an N-Cbz-protected form of L-Aspartic acid (A790024). L-Aspartic acid is a nonessential amino acid that is used to biosynthesize other amino acids within the human body. L-Aspartic acid also increases membrane conductance of mammalian neurons by voltage-dependent means, causing depolarization and nerve impulses that travel to key areas of the central nervous system.
References Anderson, H., et al.: J. Nutr., 99, 82 (1969); Honey, C., et al.: Neurosci. Lett., 61, 135 (1985); MacDonald, J., et al.: Brain Res., 237, 248 (1982)

• Marchio: TRC

Proprietà chimiche

• Peso molecolare: 267.23
• Formula: C₁₂H₁₃NO₆
• Colore/Forma: White to Off-White Solid
• InChI: InChI=1S/C11H17NO2.ClH/c1-8-9(6-7-12)4-5-10(13-2)11(8)14-3;/h4-5H,6-7,12H2,1-3H3;1H
• InChI key: InChIKey=SNXCHBXOEAIXJC-UHFFFAOYSA-N
• SMILES: COc1ccc(CCN)c(C)c1OC.Cl