🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
07350
CAS Number:
268731-07-3
Acide Fmoc-D-1,2,3,4-tétrahydronorharman-3-carboxylique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-DTπ-OH
Documents
$36.65 /1G
Taille
Request Bulk Quote
Product Information

Fmoc-D-1,2,3,4-tetrahydronorharman-3-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it a valuable tool for researchers in the fields of medicinal chemistry and biochemistry.

In addition to its role in peptide synthesis, Fmoc-D-1,2,3,4-tetrahydronorharman-3-carboxylic acid has shown potential in the development of novel therapeutic agents due to its bioactive properties. Researchers have explored its applications in the synthesis of complex natural products and pharmaceuticals, highlighting its importance in advancing drug discovery. With its favorable reactivity and stability, this compound stands out as a preferred choice for professionals seeking reliable and effective solutions in their research and development projects.

Synonyms
Fmoc-DTπ-OH
CAS Number
268731-07-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C27H22N2O4
Molecular Weight
438.46
MDL Number
MFCD01861321
PubChem ID
4523701
Melting Point
202-208 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -52,0 à -58,0° (C=1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-DTπ-OH
CAS Number
268731-07-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C27H22N2O4
Molecular Weight
438.46
MDL Number
MFCD01861321
PubChem ID
4523701
Melting Point
202-208 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -52,0 à -58,0° (C=1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-D-1,2,3,4-tetrahydronorharman-3-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in the development of compounds targeting neurological disorders, due to its structural similarity to bioactive molecules.
  • Bioconjugation: The chemical facilitates the attachment of biomolecules, such as proteins or antibodies, to various surfaces, enhancing the efficacy of drug delivery systems.
  • Analytical Chemistry: It plays a role in the development of analytical methods for detecting and quantifying complex organic compounds, improving the accuracy of results in research labs.
  • Material Science: The compound is explored in creating advanced materials with specific properties, such as increased stability and functionality, which are essential in various industrial applications.

Citations