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FMOC-D-PHE(2-I)-OH is a chemical compound that features a fluorenylmethoxycarbonyl (FMOC) protecting group attached to the amino group of the D-phenylalanine amino acid, with an additional iodine atom at the 2-position. FMOC-D-PHE(2-I)-OH plays a crucial role in the synthesis of peptides, serving as a building block for the assembly of peptide chains. The FMOC group shields the amino group from unwanted reactions, while the iodine atom provides a site for further modifications or reaction facilitation. FMOC-D-PHE(2-I)-OH is a vital component in the development of peptide-based drugs and biomolecules, utilized across various research and medical fields.

478183-65-2

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478183-65-2 Usage

Uses

Used in Pharmaceutical and Biomedical Research:
FMOC-D-PHE(2-I)-OH is used as a key building block in the synthesis of peptide-based drugs and biomolecules. Its role is crucial for the creation of specific peptide sequences that can target various biological pathways and mechanisms, contributing to the development of novel therapeutic agents.
Used in Peptide Synthesis:
FMOC-D-PHE(2-I)-OH is utilized as a protected amino acid in peptide synthesis. The FMOC protecting group ensures that the amino group remains unreactive during the synthesis process, preventing unwanted side reactions and facilitating the controlled stepwise assembly of peptide chains.
Used in Chemical Modification and Conjugation:
The iodine atom in FMOC-D-PHE(2-I)-OH serves as a point of attachment for further chemical modifications or conjugations. This feature is particularly useful in the development of bioconjugates, where peptides can be selectively linked to other molecules, such as drugs, dyes, or targeting agents, to enhance their properties or functionalities.
Used in Diagnostic and Imaging Agents:
FMOC-D-PHE(2-I)-OH can be incorporated into the design of diagnostic and imaging agents, where the iodine atom can be exploited for its radiopaque properties or as a handle for the attachment of imaging labels, enabling the visualization and tracking of biological processes in vivo.
Used in Drug Delivery Systems:
In the field of drug delivery, FMOC-D-PHE(2-I)-OH can be employed in the design of peptide-based drug carriers or targeting moieties. FMOC-D-PHE(2-I)-OH can be used to create specific peptide sequences that can selectively bind to target cells or tissues, improving the delivery and efficacy of therapeutic agents while minimizing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 478183-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,1,8 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 478183-65:
(8*4)+(7*7)+(6*8)+(5*1)+(4*8)+(3*3)+(2*6)+(1*5)=192
192 % 10 = 2
So 478183-65-2 is a valid CAS Registry Number.

478183-65-2Upstream product

478183-65-2Downstream Products

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