物质信息
ID:344484
名称和标识
IUPAC标准名
(2S)-3-amino-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
IUPAC传统名
(2S)-3-amino-2-[(tert-butoxycarbonyl)amino]propanoic acid
别名
Nα-Boc-L-β-aminoalanineNα-Boc-L-2,3-diaminopropionic acid(S)-3-氨基-2-(叔丁氧羰基氨基)丙酸(S)-2-[(tert-Butoxycarbonyl)amino]-3-aminopropionic acidNα-BOC-(S)-β-aminoalanine3-Amino-(tert-butoxycarbonyl)-L-alanine3-氨基-(叔丁氧羰基)-L-丙氨酸Nα-Boc-L-2,3-二氨基丙酸N2-tert-Butoxycarbonyl-L-2,3-diaminopropionic acidBoc-Dpr-OH(S)-3-Amino-2-(tert-butoxycarbonyl)aminopropionic acidN2-(tert-Butoxycarbonyl)-(S)-2,3-diaminopropionic acid(S)-3-Amino-2-(tert-butoxycarbonylamino)propanoic acidBoc-Dap-OH
化合物性质
安全信息
产品相关信息
杂质
~3% water
Empirical Formula (Hill Notation)
C8H16N2O4
纯度
≥98.0% (TLC)
理化性质
比旋光度
[α]20/D +5.5±1°, c = 1% in methanol: water (1:1)
熔点
210 °C (dec.)
描述信息
Other Notes
DAP 单保护衍生物；用于例如，合成氨基葡萄糖合成酶抑制剂6,7（一种肌球蛋白激酶抑制剂）。8 与金属络合基团反应制备多肽。9
包装
1, 5 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
DAP 单保护衍生物；用于例如，合成氨基葡萄糖合成酶抑制剂6,7（一种肌球蛋白激酶抑制剂）。8 与金属络合基团反应制备多肽。9
包装
1, 5 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
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