1243333-16-5

Basic information

• Product Name: (R)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,3-dimethyl-2-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)butanamide
• Synonyms: (R)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,3-dimethyl-2-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)butanamide
• CAS NO: 1243333-16-5
• Molecular Weight: 389.343
• Mol File: 1243333-16-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,3-dimethyl-2-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)butanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,3-dimethyl-2-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)butanamide(1243333-16-5)
• EPA Substance Registry System: (R)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,3-dimethyl-2-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)butanamide(1243333-16-5)

Safety Data

• Hazardous Substances Data: 1243333-16-5(Hazardous Substances Data)

Upstream product

• 70557-99-2 2-(iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 192060-34-7 N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-3-N-dimethylbutyramide 

Relevant articles and documents

Palladium-catalyzed suzuki-miyaura cross-coupling reactions of enantiomerically enriched potassium β-trifluoroboratoamides with various aryl- and hetaryl chlorides

Figure Presented. Enantiomerically enriched potassium β- trifluoroboratoamides were synthesized as air-stable solids in greater than 95:5 dr using pseudoephedrine as the chiral auxiliary. With these chiral nucleophiles, Suzuki-Miyaura cross-coupling react