FMoc-α-Me-Trp(Boc)-OH is a specialized chemical compound that integrates an N-terminal protecting group (FMoc), a C-terminal protecting group (Boc), and an alpha-methyl tryptophan residue (α-Me-Trp). FMoc-α-Me-Trp(Boc)-OH is designed for use in the synthesis of peptides, where the FMoc group shields the N-terminal amino group and the Boc group protects the C-terminal carboxyl group, facilitating controlled peptide assembly. The alpha-methyl tryptophan residue, a variant of the amino acid tryptophan with an added methyl group on the alpha carbon, imparts unique structural and functional characteristics to the peptides formed.
1315449-98-9
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Basic information
- Product Name: FMoc-α-Me-Trp(Boc)-OH
- Synonyms: (S)-N-Fmoc-N'-Boc-α-Methylpryptophan;Alfa-Me-N-Boc-N2(Fmoc)-Try-OH;(S)-FMOC-ALPHA-METHYL-N-BOC-TRYPTOPHAN
- CAS NO:1315449-98-9
- Molecular Formula: C32H32N2O6
- Molecular Weight: 540.60628
- EINECS: N/A
- Product Categories: α-Methyl Amino Acids
- Mol File: 1315449-98-9.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: 1.25±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 3.79±0.11(Predicted)
- CAS DataBase Reference: FMoc-α-Me-Trp(Boc)-OH(CAS DataBase Reference)
- NIST Chemistry Reference: FMoc-α-Me-Trp(Boc)-OH(1315449-98-9)
- EPA Substance Registry System: FMoc-α-Me-Trp(Boc)-OH(1315449-98-9)
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Safety Data
- Hazard Codes: F,T
- Statements: 14/15-24/25-34
- Safety Statements: 26-36/37/39-43-45
- WGK Germany:
- RTECS:
- TSCA: No
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1315449-98-9(Hazardous Substances Data)
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1315449-98-9 Usage
Uses
Used in Peptide Synthesis:FMoc-α-Me-Trp(Boc)-OH serves as a crucial building block in the synthesis of peptides, contributing to the creation of sequences with tailored properties. Its incorporation allows for the development of peptides with specific structural requirements and functionalities, which can be essential for various biological and pharmaceutical applications.
Used in Research and Development:
In the scientific community, FMoc-α-Me-Trp(Boc)-OH acts as a valuable research tool, particularly in the investigation of protein-ligand interactions. It aids in understanding how peptides interact with other molecules, which is fundamental for drug development. By examining these interactions, researchers can gain insights into the mechanisms of action for potential therapeutic agents and optimize their design for improved efficacy and selectivity.
Used in Pharmaceutical Industry:
FMoc-α-Me-Trp(Boc)-OH is utilized in the pharmaceutical industry for the development of drugs with specific targeting and therapeutic properties. FMoc-α-Me-Trp(Boc)-OH's role in peptide synthesis allows for the creation of drugs that can be tailored to interact with particular biological targets, potentially leading to more effective treatments with fewer side effects.
Used in Biochemical Research:
FMoc-α-Me-Trp(Boc)-OH is also applied in biochemical research to explore the roles and mechanisms of peptides in biological systems. This can include studying the effects of modified peptides on cellular processes, signaling pathways, and the overall regulation of biological functions, thereby contributing to a broader understanding of peptide-based therapeutics and their potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1315449-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,4,4 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.Calculate Digit Verification of CAS Registry Number 1315449-98:
(9*1)+(8*3)+(7*1)+(6*5)+(5*4)+(4*4)+(3*9)+(2*9)+(1*8)=159
159 % 10 = 9
So 1315449-98-9 is a valid CAS Registry Number.
1315449-98-9Upstream product
1315449-98-9Downstream Products
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FMoc-α-Me-Trp(Boc)-OH
