105089-61-0

Basic information

• Product Name: L-Phenylalanine, N-acetyl-4-iodo-, methyl ester
• CAS NO: 105089-61-0
• Molecular Formula: C12H14INO3
• Molecular Weight: 347.153
• Mol File: 105089-61-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-acetyl-4-iodo-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-acetyl-4-iodo-, methyl ester(105089-61-0)
• EPA Substance Registry System: L-Phenylalanine, N-acetyl-4-iodo-, methyl ester(105089-61-0)

Safety Data

• Hazardous Substances Data: 105089-61-0(Hazardous Substances Data)

Upstream product

• 1991-81-7 p-iodophenylalanine 
• 108-24-7 acetic anhydride 
• 77-76-9 2,2-dimethoxy-propane 
• 1991-81-7 4-iodo-L-phenylalanine 
• 113850-77-4 (S)-methyl 2-amino-3-(4-iodophenyl)propanoate 
• 127-09-3 sodium acetate 
• 3618-96-0 (S)-N-acetylphenylalanine 
• 1173918-59-6 methyl 2-amino-3-(4-iodophenyl)propanoate hydrochloride 
• 105089-60-9 2-Acetylamino-3-(4-trimethylsilanyl-phenyl)-propionic acid methyl ester 

Downstream Products

• 219826-18-3 N-acetyl 4-C-(3,7-anhydro-4,5,6,8-tetra-O-acetyl-1,1,2,2-tetradehydro-1,2-D-glycero-D-galactooctityl)-DL-phenylalanine methyl ester 
• 219826-20-7 N-acetyl 4-C-(3,7-anhydro-4,5,6,8-tetra-O-acetyl-1,1,2,2-tetradehydro-1,2-D-glycero-D-talooctityl)-DL-phenylalanine methyl ester 
• 219826-16-1 N-acetyl 4-C-(3,7-anhydro-4,5,6,8-tetra-O-acetyl-1,1,2,2-tetradehydro-1,2-D-glycero-D-mannooctityl)-DL-phenylalanine methyl ester 
• 288160-50-9 N-acetyl-p-(diphenylphosphino)-L-phenylalanine metyl ester 
• 900521-56-4 methyl (2S)-2-acetamido-3-(4-trimethylstannylphenyl)propanoate 
• 1612798-70-5 C₁₆H₂₀INO₇ 
• 219826-24-1 N-acetyl 4-C-(3,7-anhydro-1,1,2,2-tetradehydro-1,2-D-glycero-D-mannooctityl)-DL-phenylalanine 
• 219826-32-1 4-C-(3,7-anhydro-1-oxo-1,2-D-glycero-D-galactooctit-1-yl)-DL-phenylalanine 

Relevant articles and documents

Copper-catalyzed [18F]fluorination of (Mesityl)(aryl)iodonium salts

A practical, rapid, and highly regioselective Cu-catalyzed radiofluorination of (mesityl)(aryl)iodonium salts is described. This protocol utilizes [18F]KF to access 18F-labeled electron-rich, -neutral, and -deficient aryl fluorides under a single set of mild conditions. This methodology is applied to the synthesis of protected versions of two important radiotracers: 4-[18F]fluorophenylalanine and 6-[ 18F]fluoroDOPA.

Synthesis of novel N-protected hydrophobic phenylalanines and their application in potential antibacterials

An efficient synthesis of two new N-acetyl-4′-arylphenylalanines is described together with their incorporation into a number of cationic peptoid antibacterial agents, one of which had an MIC of 7.8 μg/mL against Staphylococcus aureus. Crown Copyright

PEPTIDIC COMPOUNDS

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