330-45-0

Basic information

• Product Name: L-Phenylalanine, N-acetyl-3-fluoro-
• CAS NO: 330-45-0
• Molecular Formula: C11H12FNO3
• Molecular Weight: 225.22
• Mol File: 330-45-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-acetyl-3-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-acetyl-3-fluoro-(330-45-0)
• EPA Substance Registry System: L-Phenylalanine, N-acetyl-3-fluoro-(330-45-0)

Safety Data

• Hazardous Substances Data: 330-45-0(Hazardous Substances Data)

Upstream product

• 599178-62-8 C₁₁H₁₀FNO₃ 
• 380-70-1 diethyl α-acetamido, α-(3-fluorobenzyl)malonate 
• 17607-28-2 N-acetyl-3-fluoro-D,L-phenylalanine 
• 100-63-0 phenylhydrazine 

Downstream Products

• 110117-84-5 (R)-2-amino-3-(3-fluorophenyl)propionic acid 

Relevant articles and documents

DEVICE AND METHOD FOR EVALUATING ORGANIC MATERIAL FOR ORGANIC SOLAR CELL

Provided are a novel 1,2-bis(dialkylphosphino)-4,5-(methylenedioxy)benzene derivative that forms a metal complex having particularly high asymmetry induction capacity and catalytic activity on β-dehydroamino acids, a method for manufacturing the same, a metal complex having this 1,2-bis(dialkylphosphino)-4,5-(methylenedioxy)benzene derivative as a ligand, and an asymmetric hydrogenation method using this metal complex. A 1,2-bis(dialkylphosphino)-4,5-(methylenedioxy)benzene derivative represented by general formula (1). (In the formula, R1 and R2 represent an alkyl group having 1-10 carbon atoms, and R1 and R2 have different numbers of carbon atoms.)

Three-hindered quadrant phosphine ligands with an aromatic ring backbone for the rhodium-catalyzed asymmetric hydrogenation of functionalized alkenes

The three-hindered quadrant phosphine ligands (R)-1-tert- butylmethylphosphino-2-(di-tert-butylphosphino)benzene ((R)-3H-BenzP*) and (R)-2-tert-butylmethylphosphino-3-(di-tert-butylphosphino)quinoxaline ((R)-3H-QuinoxP*) exhibited good to excellent enantioselectivities in the rhodium-catalyzed asymmetric hydrogenation of selected dehydroamino acid derivatives, enamides, and ethenephosphonates.

Enantiopure 1,2-Bis(tert-butylmethylphosphino)benzene as a highly efficient ligand in rhodium-catalyzed asymmetric hydrogenation

Figure Presented. An electron-rich P-stereogenic bisphosphine ligand named "BenzP" was conveniently prepared from o-dibromobenzene and enantiopure tert-butylmethylphosphine-borane. Its rhodium complex exhibited excellent enantioselectivities of up to 99.9% and high catalytic activity of up to 10000 h-1 TOF in asymmetric hydrogenations of various functionalized alkenes.