1370470-92-0

Basic information

• Product Name: {3-[(S)-4-isopropyl-4,5-dihydrooxazol-2-yl]-1-[(S)-tetrahydro-2H-pyran-2-yl]-1H-indol-2-yl}diphenylphosphane oxide
• CAS NO: 1370470-92-0
• Molecular Weight: 512.588
• Mol File: 1370470-92-0.mol

Chemical Properties

• CAS DataBase Reference: {3-[(S)-4-isopropyl-4,5-dihydrooxazol-2-yl]-1-[(S)-tetrahydro-2H-pyran-2-yl]-1H-indol-2-yl}diphenylphosphane oxide(CAS DataBase Reference)
• NIST Chemistry Reference: {3-[(S)-4-isopropyl-4,5-dihydrooxazol-2-yl]-1-[(S)-tetrahydro-2H-pyran-2-yl]-1H-indol-2-yl}diphenylphosphane oxide(1370470-92-0)
• EPA Substance Registry System: {3-[(S)-4-isopropyl-4,5-dihydrooxazol-2-yl]-1-[(S)-tetrahydro-2H-pyran-2-yl]-1H-indol-2-yl}diphenylphosphane oxide(1370470-92-0)

Safety Data

• Hazardous Substances Data: 1370470-92-0(Hazardous Substances Data)

Upstream product

• 3136-02-5 2-chlorotetrahydro-2H-pyran 
• 1370470-84-0 (S)-2-{2-(diphenylphosphanyl)-1-[(S)-tetrahydro-2H-pyran-2-yl]-1H-indol-3-yl}-4-isopropyl-4,5-dihydrooxazole 
• 110-87-2 3,4-dihydro-2H-pyran 

Relevant articles and documents

N1-functionalized indole-phosphane oxazoline (IndPHOX) ligands in asymmetric allylic substitution reactions

N-Functionalized IndPHOX ligands bearing various groups have been synthesized and the effects of the N1-substituent on the reaction rate, yield, and asymmetric induction in a palladium-catalyzed allylic substitution reaction are reported. The p