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Catalog Number:
29653
CAS Number:
1076196-98-9
Fmoc-5-amino-2,4-dimethoxy-benzoic acid
Purity:
≥ 98% (HPLC)
Documents
$100.05 /25MG
Pack Size Availability Price
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Product Information

Fmoc-5-amino-2,4-dimethoxy-benzoic acid is a versatile compound widely utilized in peptide synthesis and drug discovery. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability and ease of handling during the synthesis process. Its unique structure allows for selective deprotection, making it an ideal choice for researchers looking to streamline their workflows in solid-phase peptide synthesis. The presence of methoxy groups enhances its solubility and reactivity, facilitating its application in various organic reactions and modifications.

In addition to its role in peptide synthesis, Fmoc-5-amino-2,4-dimethoxy-benzoic acid is also valuable in the development of pharmaceuticals and biologically active compounds. Its ability to serve as a building block in the construction of complex molecules opens up avenues for innovation in medicinal chemistry. Researchers can leverage its properties to create targeted therapies and study biological interactions, making it a crucial component in the toolkit of modern chemists and biochemists.

CAS Number
1076196-98-9
Purity
≥ 98% (HPLC)
Molecular Formula
C24H21NO6
Molecular Weight
419.43
MDL Number
MFCD11226790
PubChem ID
45356711
Melting Point
213-219 °C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
CAS Number
1076196-98-9
Purity
≥ 98% (HPLC)
Molecular Formula
C24H21NO6
Molecular Weight
419.43
MDL Number
MFCD11226790
PubChem ID
45356711
Melting Point
213-219 °C
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-5-amino-2,4-dimethoxy-benzoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in the development of peptide-based drugs, enhancing their stability and bioavailability.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Cancer Therapy: Its derivatives are being explored in cancer research for their potential to selectively target and inhibit tumor growth, offering a promising avenue for new treatments.
  • Analytical Chemistry: The compound is utilized in analytical methods for the detection and quantification of biomolecules, aiding researchers in understanding complex biological systems.

Citations