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Catalog Number:
29196
CAS Number:
135807-51-1
Boc-(2-aminophenyl)acetic acid
Purity:
≥ 99% (HPLC)
Documents
$72.31 /1G
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Product Information

Boc-(2-aminophenyl)acetic acid is a versatile compound widely utilized in pharmaceutical research and organic synthesis. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, making it an essential intermediate in the synthesis of various bioactive molecules. Its unique structure allows for the selective modification of the amino group, facilitating the development of novel pharmaceuticals and therapeutic agents. Researchers appreciate its role in peptide synthesis and drug design, particularly in the creation of compounds with enhanced bioavailability and targeted action.

In addition to its applications in drug development, Boc-(2-aminophenyl)acetic acid serves as a valuable building block in the synthesis of agrochemicals and fine chemicals. Its stability and reactivity make it suitable for various coupling reactions, enabling the formation of complex molecular architectures. This compound's ability to enhance solubility and improve pharmacokinetic properties positions it as a preferred choice for researchers aiming to innovate in medicinal chemistry and related fields.

CAS Number
135807-51-1
Purity
≥ 99% (HPLC)
Molecular Formula
C13H17NO4
Molecular Weight
251.28
MDL Number
MFCD09750482
PubChem ID
17890355
Appearance
White to pale pink solid
Conditions
Store at 0-8 °C
General Information
CAS Number
135807-51-1
Purity
≥ 99% (HPLC)
Molecular Formula
C13H17NO4
Molecular Weight
251.28
MDL Number
MFCD09750482
PubChem ID
17890355
Appearance
White to pale pink solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(2-aminophenyl)acetic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders. Its structure allows for modifications that enhance drug efficacy.
  • Peptide Synthesis: It acts as a protecting group for amines in peptide synthesis, facilitating the formation of complex peptide structures while preventing unwanted reactions.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules to therapeutic agents, which is crucial in developing targeted drug delivery systems.
  • Research in Organic Chemistry: It is used in organic synthesis as a building block, enabling chemists to explore new reactions and develop innovative compounds with potential applications in various fields.
  • Analytical Chemistry: Boc-(2-aminophenyl)acetic acid is utilized in analytical methods to study the behavior of amino acids and their derivatives, providing insights into protein structure and function.

Citations