Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
31665
CAS Number:
725728-43-8
Acide ( R )-Fmoc-2-amino-2-méthyl-3-tritylsulfanyl-propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-α-Me-L-Cys(Trt)-OH
Documents
$125.80 /25 mg
Taille
Request Bulk Quote
Product Information

(R)-Fmoc-2-amino-2-methyl-3-tritylsulfanyl-propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective deprotection of amino acids during solid-phase peptide synthesis. Its trityl sulfanyl group enhances stability and solubility, making it an ideal choice for researchers focused on synthesizing complex peptides and proteins.

In addition to its applications in peptide chemistry, this compound is also valuable in the development of pharmaceuticals, particularly in the design of novel therapeutics that require precise amino acid sequences. Its ability to provide a stable and reactive platform for further chemical modifications allows for the exploration of diverse biological activities. Researchers and industry professionals can leverage (R)-Fmoc-2-amino-2-methyl-3-tritylsulfanyl-propionic acid to streamline their synthesis processes and enhance the efficiency of their projects.

Synonyms
Fmoc-α-Me-L-Cys(Trt)-OH
CAS Number
725728-43-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 38 H 33 NON 4 S
Molecular Weight
599.74
MDL Number
MFCD30749166
PubChem ID
72804209
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 45 ± 8 º (C = 0,25 dans CH 3 OH) D 20 = 69 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-α-Me-L-Cys(Trt)-OH
CAS Number
725728-43-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 38 H 33 NON 4 S
Molecular Weight
599.74
MDL Number
MFCD30749166
PubChem ID
72804209
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 45 ± 8 º (C = 0,25 dans CH 3 OH) D 20 = 69 ± 2 º (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

(R)-Fmoc-2-amino-2-methyl-3-tritylsulfanyl-propionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing peptide-based drugs, enhancing the stability and bioavailability of therapeutic agents.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of peptides to various biomolecules, which is crucial for creating targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies related to neuropeptides, helping researchers understand the role of peptides in neurological functions and disorders.
  • Custom Synthesis Services: Many contract research organizations utilize this compound for custom synthesis projects, providing tailored solutions for clients in academia and industry.

Citations