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CAS 10270-94-7

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H-Dab(Boc)-OH

Description:
H-Dab(Boc)-OH, also known as N-Boc-2,3-diaminobutyric acid, is a chemical compound characterized by its structure, which includes a protected amine group and a carboxylic acid functional group. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amine, allowing for selective reactions without affecting the amine functionality. This compound is typically used in peptide synthesis and other organic synthesis applications, where the protection of amines is crucial for controlling reactivity. H-Dab(Boc)-OH is soluble in polar organic solvents, making it suitable for various synthetic procedures. Its stability under standard laboratory conditions allows for ease of handling and storage. Additionally, the presence of both amine and carboxylic acid functionalities makes it a versatile building block in the synthesis of more complex molecules, particularly in the field of medicinal chemistry and drug development. As with many chemical substances, proper safety precautions should be observed when handling H-Dab(Boc)-OH to mitigate any potential hazards.
Formula:C9H18N2O4
Synonyms:
  • (S)-2-Amino-4-(Boc-amino)butanoic acid
  • Nγ-Boc-L-2,4-diaminobutyric acid≥ 99% (HPLC)
  • N-GAMMA-T-BUTOXYCARBONYL-L-ALPHA,GAMMA-DIAMINOBUTYRIC ACID
  • (2S)-2-amino-4-{[(tert-butoxy)carbonyl]amino}butanoic acid
  • (2S)-2-Amino-4-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-Butanoic Acid
  • H-DAB(BOC)-OH
  • (2S)-Amino-4-[(tert-butoxycarbonyl)amino]butanoic acid
  • N-GAMMA-BOC-L-2,4-DIAMINOBUTYRIC ACID
  • L-Dab(Boc)-OH
  • Butanoic acid, 2-amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-
  • See more synonyms
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