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Catalog Number:
31666
CAS Number:
1151854-06-6
Fmoc-L-Tyr( SO3DCV )-OH
Purity:
≥ 98 % (HPLC)
Documents
$79.22 /25 mg
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Product Information

Fmoc-L-Tyr(SO3DCV)-OH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique sulfonyl group, enhancing its reactivity and making it an excellent choice for researchers focused on developing novel therapeutic peptides. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex biomolecules. The compound's distinctive properties make it particularly valuable in the fields of medicinal chemistry and biochemistry, where precision and efficiency are paramount.

Researchers and industry professionals can leverage Fmoc-L-Tyr(SO3DCV)-OH in various applications, including the design of targeted drug delivery systems and the development of peptide-based therapeutics. Its ability to improve solubility and stability in biological environments enhances the potential for successful drug formulation. Additionally, the compound's unique structure allows for the introduction of specific functionalities, making it a versatile tool in the synthesis of bioactive compounds. With its practical applications and benefits, Fmoc-L-Tyr(SO3DCV)-OH is an essential asset for advancing research in peptide chemistry.

CAS Number
1151854-06-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H21Cl2NO8S
Molecular Weight
578.42
MDL Number
MFCD26408195
PubChem ID
169545597
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -24,6 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1151854-06-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H21Cl2NO8S
Molecular Weight
578.42
MDL Number
MFCD26408195
PubChem ID
169545597
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -24,6 ± 1 ° (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-L-Tyr(SO3DCV)-OH 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). Its protective group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. The unique structure aids in the development of therapeutics targeting specific biological pathways, offering potential advantages over traditional small molecules.
  • Bioconjugation: The chemical is employed in bioconjugation processes, where it can be attached to biomolecules for targeted delivery systems. This application is crucial in creating more effective drug delivery mechanisms.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems by facilitating the synthesis of neuropeptides, which are vital for understanding brain function and developing treatments for neurological disorders.
  • Custom Synthesis Services: Many research institutions and companies utilize this compound for custom synthesis projects, allowing for tailored solutions in various applications, from academic research to industrial production.

Citations