146476-36-0

Basic information

• Product Name: Carbamic acid, [1-[(diphenylphosphino)methyl]-2-phenylethyl]-, 1,1-dimethylethyl ester, (S)-
• CAS NO: 146476-36-0
• Molecular Formula: C26H30NO2P
• Molecular Weight: 419.503
• Mol File: 146476-36-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [1-[(diphenylphosphino)methyl]-2-phenylethyl]-, 1,1-dimethylethyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [1-[(diphenylphosphino)methyl]-2-phenylethyl]-, 1,1-dimethylethyl ester, (S)-(146476-36-0)
• EPA Substance Registry System: Carbamic acid, [1-[(diphenylphosphino)methyl]-2-phenylethyl]-, 1,1-dimethylethyl ester, (S)-(146476-36-0)

Safety Data

• Hazardous Substances Data: 146476-36-0(Hazardous Substances Data)

Upstream product

• 126301-19-7 (2S)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropyl methanesulfonate 
• 15475-27-1 potassium diphenylphosphine 
• 63-91-2 L-phenylalanine 
• 3182-95-4 L-Phenylalaninol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 141403-49-8 (2S)-2-[N-(tert-butoxycarbonyl)amino]-3-phenyl-O-(4-methylphenylsulfonyl)propan-1-ol 
• 4522-04-7 ethyl N-{[(1,1-dimethylethyl)oxy]carbonyl}-L-phenylalaninate 
• 66605-57-0 (S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol 
• 829-85-6 diphenylphosphane 

Downstream Products

• 920760-41-4 ((S)-1-Benzyl-2-diphenylphosphanyl-ethyl)-methyl-amine 
• 146476-38-2 (S)-1-(diphenylphosphino)-3-phenylpropan-2-amine 

Relevant articles and documents

Asymmetric kinetic resolution of sulfides for the construction of unsymmetric sulfides and chiral 3,3-disubstituted oxindoles

A range of 3,3-disubstituted oxindoles accessed using para-quinone methides derived from isatins with thiols were used for the formation of unsymmetrical disulfides, and 3,3-disubstituted oxindoles with a chiral quaternary carbon center and unsymmetric di

Catalytic asymmetric [4+2] annulation initiated by an aza-rauhut-currier reaction: Facile entry to highly functionalized tetrahydropyridines

Under control: The first example of chiral amino phosphine catalysts for the title reaction between vinyl ketones and N-sulfonyl-1-aza-1,3-dienes has been developed. Under ambient conditions, this protocol provides straightforward access to densely functionalized, enantioenriched tetrahydropyridines with high levels of sterecontrol in good to excellent yields. Copyright

Design and synthesis of new bidentate phosphoramidite ligands for enantioselective copper-catalyzed conjugate addition of diethylzinc to enones

Several thioaryl- and phosphino-phosphoramidite ligands have been synthesized from commercially available β-aminoalcohols. This new family of bidentate ligands are highly active in the enantioselective copper-catalyzed conjugate addition of diethylzinc to