(N-Boc-β-amino)-Ala-OH

• Catalog No.: 662836
• CAS Number: 73259-81-1
• M. F.: C8H16N2O4
• M. W.: 204.22364

SYNONYMS

• Title: (N-Boc-β-氨基)-丙氨酸
• IUPAC name: (2S)-3-amino-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
• IUPAC Traditional name: (2S)-3-amino-2-[(tert-butoxycarbonyl)amino]propanoic acid
• Synonyms: (S)-3-氨基-2-(叔丁氧羰基氨基)丙酸; (S)-3-Amino-2-(tert-butoxycarbonylamino)propanoic acid; (S)-2-[(tert-Butoxycarbonyl)amino]-3-aminopropionic acid; (S)-3-Amino-2-(tert-butoxycarbonyl)aminopropionic acid; Nα-BOC-(S)-β-aminoalanine; Nα-Boc-L-β-aminoalanine; N2-(tert-Butoxycarbonyl)-(S)-2,3-diaminopropionic acid; N2-tert-Butoxycarbonyl-L-2,3-diaminopropionic acid; Boc-Dap-OH; Boc-Dpr-OH; 3-Amino-(tert-butoxycarbonyl)-L-alanine; Nα-Boc-L-2,3-diaminopropionic acid; 3-氨基-(叔丁氧羰基)-L-丙氨酸; Nα-Boc-L-2,3-二氨基丙酸

DATABASE IDS

• PubChem SID: 24884604
• CAS Number: 73259-81-1
• MDL Number: MFCD00236843
• Beilstein Number: 4182136

PROPERTIES

• Empirical Formula (Hill Notation): C8H16N2O4
• Melting Point: 210 °C (dec.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application
Reactant for:
• Protein assembly directed by synthetic molecular recognition motifs1
• Solid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activities2
• Synthesis of HCV protease inhibitor modified analogs3
• Solid phase synthesis of peptidic V1a receptor agonists4
• Directed peptide assembly at lipid-water interface5

Description (简体中文)

包装
1 g in glass bottle
Application
Reactant for:
• Protein assembly directed by synthetic molecular recognition motifs1
• Solid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activities2
• Synthesis of HCV protease inhibitor modified analogs3
• Solid phase synthesis of peptidic V1a receptor agonists4
• Directed peptide assembly at lipid-water interface5