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Catalog Number:
04056
CAS Number:
112898-24-5
Ácido 2 S ,3 R -3-(Boc-amino)-2-hidroxi-4-(4-nitrofenil)butírico
Purity:
≥ 99 % (TLC)
Synonym(s):
Boc-( 2S , 3R- AHNPB-OH
Documents
$60.39 /5 mg
Tamaño
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Product Information

The compound (2S,3R)-3-(Boc-amino)-2-hydroxy-4-(4-nitrophenyl)butyric acid is a versatile building block in pharmaceutical and biochemical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is widely used in peptide synthesis, allowing for the selective protection of amino groups during complex organic reactions. Its unique structure, which includes a nitrophenyl moiety, enhances its potential as a precursor in the development of bioactive molecules, particularly in the synthesis of novel pharmaceuticals targeting various biological pathways.

Researchers and industry professionals can leverage this compound in drug discovery and development, particularly in the design of inhibitors or modulators for specific enzymes or receptors. Its ability to undergo further functionalization makes it an attractive candidate for creating diverse chemical libraries. Additionally, the compound's stability and compatibility with various reaction conditions facilitate its use in both academic and industrial settings, making it a valuable asset for those engaged in medicinal chemistry and related fields.

Synonyms
Boc-( 2S , 3R- AHNPB-OH
CAS Number
112898-24-5
Purity
≥ 99 % (TLC)
Molecular Formula
C15H20N2O7
Molecular Weight
340.3
MDL Number
MFCD00058524
PubChem ID
4123011
Appearance
Polvo ligeramente verde
Optical Rotation
[a] D 20 = +67,5 ± 2º (C=1 en MeOH)
Conditions
Conservar a -0°C
General Information
Synonyms
Boc-( 2S , 3R- AHNPB-OH
CAS Number
112898-24-5
Purity
≥ 99 % (TLC)
Molecular Formula
C15H20N2O7
Molecular Weight
340.3
MDL Number
MFCD00058524
PubChem ID
4123011
Appearance
Polvo ligeramente verde
Optical Rotation
[a] D 20 = +67,5 ± 2º (C=1 en MeOH)
Conditions
Conservar a -0°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S,3R)-3-(Boc-amino)-2-hydroxy-4-(4-nitrophenyl)butyric acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting metabolic disorders.
  • Biochemical Research: It is used in studies involving enzyme inhibition and protein interactions, helping researchers understand biological pathways and mechanisms.
  • Drug Delivery Systems: Its unique properties allow for the formulation of advanced drug delivery systems, enhancing the bioavailability and efficacy of therapeutic agents.
  • Analytical Chemistry: The compound is employed in analytical techniques to detect and quantify specific biomolecules, making it valuable in quality control processes.
  • Material Science: It is explored in the development of novel materials with specific chemical functionalities, which can be applied in coatings and adhesives.

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