CAS 78603-91-5
:α-[(1S)-1-Aminoetil]-α-fenilbenzenometanol
- (2S)-2-amino-1,1-diphenylpropan-1-ol
- (S)-β-Hydroxy-α-methyl-β-phenylbenzeneethanamine
- 1,1-Diphenyl-L-alaninol
- 2-Amino-1,1-Diphenylpropan-1-Ol
- Benzenemethanol, α-(1-aminoethyl)-α-phenyl-, (S)-
- Benzenemethanol, α-[(1S)-1-aminoethyl]-α-phenyl-
- α-[(1S)-1-Aminoethyl]-α-phenylbenzenemethanol
- (S)-2-Amino-1,1-diphenyl-1-propanol
- (S)-2-Amino-1,1-diphenyl-1-propanol
(S)-2-Amino-1,1-diphenyl-1-propanol
CAS:Fórmula:C15H17NOPureza:97%Cor e Forma:SolidPeso molecular:227.3016(S)-(+)-2-Amino-1,1-diphenyl-1-propanol
CAS:(S)-(+)-2-Amino-1,1-diphenyl-1-propanolFórmula:C15H17NOPureza:97%Cor e Forma: yellow solidPeso molecular:227.30g/mol(S)-2-Amino-1,1-diphenylpropan-1-ol
CAS:Fórmula:C15H17NOPureza:98%Cor e Forma:SolidPeso molecular:227.307(S)-2-Amino-1,1-diphenyl-1-propanol
CAS:Produto ControladoApplications (S)-2-AMINO-1,1-DIPHENYL-1-PROPANOL (cas# 78603-91-5) is a useful research chemical.
Fórmula:C15H17NOCor e Forma:NeatPeso molecular:227.3(S)-(-)-2-Amino-1,1-diphenyl-1-propanol
CAS:L-2-Amino-1,1-diphenyl-1-propanol is a chiral, catalytic reagent that is used in organic chemistry for the asymmetric synthesis of alcohols and other molecules. The L form of this compound can be prepared from phenylacetic acid by an alkylation reaction with propanolamine in the presence of palladium catalyst. This substance has been shown to have anthelminthic properties. It has also been shown to have a strong interaction with aminoalcohols. L-2-Amino-1,1-diphenyl-1-propanol can alkylate aromatic ketones and vicinal diols by utilizing its catalytic activity. Elemental analysis indicates that this substance contains only carbon, hydrogen, nitrogen and oxygen.
Fórmula:C15H17NOPureza:Min. 95%Cor e Forma:White PowderPeso molecular:227.3 g/molRef: 3D-FA74897
Produto descontinuado





