N-Boc-L-phenylalaninal N-Boc-L-苯丙氨醛

CAS 72155-45-4 MFCD00143854

化学结构图

72155-45-4
SMILES: CC(C)(C)OC(=O)N[C@@H](CC1C=CC=CC=1)C=O

化学属性

Mol. FormulaC6H5CH2CH[NHCO2C(CH3)3]CHO
Mol. Weight249.31
Melting Point86-88 °C(lit.)

别名和识别编码

Chemical NameN-Boc-L-phenylalaninal
CAS Number72155-45-4
Synonym N-[(1S)-1-Formyl-2-phenylethyl]carbamic Acid 1,1-Dimethylethyl Ester N-Boc-L-苯丙氨醛 (S)-(-)-2-(叔丁氧羰基氨基)-3-苯丙醛
MDL NumberMFCD00143854
PubChem Substance ID24870581
Chemical Name TranslationN-Boc-L-苯丙氨醛
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分类

  • {SA} Aldehydes, Amino Acid Derivatives, Amino Aldehydes, Application Index, B, Bioactive Sm
  • {SNA} Aldehydes, Amino Acids & Derivatives, Amino Aldehydes, Application Index, Building Blocks, Building Blocks for HIV Protease Inhibitors, C13-C60, Carbonyl Compounds, Cell Signaling Enzymes, Chemical Biology, Chemical Synthesis, HIV Protease Reagents & Envelope Proteins, Organic Building Blocks, Peptide Chemistry, 生化试剂, 酶、抑制剂和底物
  • Aldehydes, Amino Acid Derivatives, Amino Aldehydes, Application Index,

产品应用

  • An amino aldehyde. A potent human cathepsin K inhibitor.

相关文献及参考

  • Catalano, J.G., et al.:
  • 1. Mordini, A. et al. Tetrahedron Lett. 37 , 5209, (1996)

安全信息

WGK Germany3

系列性分类

  1. Chemical Synthesis 化学合成
  2. Building Blocks 合成砌块
  3. Organic Building Blocks 有机砌块
  4. Carbonyl Compounds 羰基化合物
  5. Aldehydes - Carbonyl Compounds
  6. C13-C60 - Aldehydes
  1. Chemical Synthesis 化学合成
  2. Chemical Biology 生物化学
  3. Peptide Chemistry 多肽化学
  4. Amino Acid Derivatives 氨基酸及其衍生物
  5. Amino Aldehydes - Amino Acid Derivatives
  1. Life Science 生命科学
  2. Biochemicals and Reagents 生化试剂
  3. Amino Acids 氨基酸
  4. Modified Amino Acids - Amino Acids
  5. Boc-amino Acids

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