Boc-Phe(4-I)-NH2
Product Specifications
| CAS Number | 868694-44-4 |
|---|---|
| Molecular Formula | C14H19IN2O3 |
| Molecular Weight | 390.22 |
| Purity | ≥99.0% |
| Appearance | White to off-white solid |
| Storage Conditions | 2-8°C |
| Package | From 100g/bottle to 25kg/drum |
Product Overview
CAS 868694-44-4 tert-Butyl [(S)-1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl]carbamate (also commonly known as Boc-Phe(4-I)-NH2 or (S)-tert-butyl (1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl)carbamate).
Applications
Derivatized Amino Acid: This molecule is the C-terminal primary amide derivative of 4-iodo-L-phenylalanine, featuring an N-terminal Boc (tert-butoxycarbonyl) protecting group.
Medicinal Chemistry & Peptidomimetics: Commonly used as a protected intermediate/building block for constructing peptide sequences or peptidomimetic compounds terminated with an amide group.
Transition-Metal Coupling Partner: The aromatic iodine (aryl iodide) handle provides a functional handle for palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Sonogashira, or Heck couplings) to append modified aromatic rings,alkynes, or alkenes directly onto the peptide backbone.
Quality Assurance
Can be tested according to the customer’s method of analysis.
Certificate of Analysis (COA) and Material Safety Data Sheets (MSDS) provided upon request.
