232618-88-1

Basic information

• Product Name: (2R,5S)-2-dimethylamino-3-phenyl-1,3-diazaphosphabicyclo[3.3.0^1,5]octane
• Synonyms: (2R,5S)-2-dimethylamino-3-phenyl-1,3-diazaphosphabicyclo[3.3.0^1,5]octane
• CAS NO: 232618-88-1
• Molecular Weight: 249.296
• Mol File: 232618-88-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (2R,5S)-2-dimethylamino-3-phenyl-1,3-diazaphosphabicyclo[3.3.0^1,5]octane(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,5S)-2-dimethylamino-3-phenyl-1,3-diazaphosphabicyclo[3.3.0^1,5]octane(232618-88-1)
• EPA Substance Registry System: (2R,5S)-2-dimethylamino-3-phenyl-1,3-diazaphosphabicyclo[3.3.0^1,5]octane(232618-88-1)

Safety Data

• Hazardous Substances Data: 232618-88-1(Hazardous Substances Data)

Upstream product

• 64030-44-0 (2S)-2-(anilinomethyl)pyrrolidine 
• 1608-26-0 Hexamethylphosphorous triamide 
• 68295-47-6 (S)-5-oxo-N-phenylpyrrolidine-2-carboxamide 
• 62-53-3 aniline 
• 56-86-0 L-glutamic acid 

Downstream Products

• 1012370-61-4 C₂₉H₂₇N₂OP 
• 1012370-62-5 C₂₇H₂₅N₂OP 
• 1012370-60-3 C₂₅H₂₇N₂OP 
• 735278-40-7 C₁₂H₁₇N₂OP 
• 735278-45-2 1-phenoxy-2-phenyl-hexahydro-pyrrolo[1,2-c][1,3,2]diazaphopsphole 
• 1012370-61-4 C₂₉H₂₇N₂OP 
• 1012370-59-0 1-(biphenyl-2-yloxy)-2-phenyl-hexahydro-pyrrolo[1,2-c][1,3,2]diazaphopsphole 
• 1012370-62-5 C₂₇H₂₅N₂OP 
• 1012370-60-3 C₂₅H₂₇N₂OP 
• 735278-40-7 C₁₂H₁₇N₂OP 
• 207129-48-4 (2S,5S)-2-(2-hydroxyphenyl)-3-phenyl-1,3-diaza-2-phosphabicyclo[3.3.0]octane 2-oxide 
• 261162-68-9 (1S,3aS)-1-Phenoxy-2-phenyl-hexahydro-pyrrolo[1,2-c][1,3,2]diazaphosphole 1-oxide 

Relevant articles and documents

New chiral organophosphorus derivatizing agent for the determination of enantiomeric composition of chloro- and bromohydrins by 31P NMR spectroscopy

The synthesis of a new chiral organophosphorus derivatizing agent prepared from (S)-2-anilinomethylpyrrolidine 1 and its successful use in the determination of enantiomeric composition of various halohydrins by 31P NMR spectroscopy is described

On the role of PIII ligands in the conjugate addition of diorganozinc derivatives to enones

A mechanistic study on the conjugate addition of diethylzinc to cyclohexenone catalyzed by various chiral PIII ligands, provides new insights into its mechanism. Complete in situ conversion of the catalytic amount of Cu(OTf)2 into Cu

A practical method for the large-scale synthesis of diastereomerically pure (2R,5S)-3-phenyl-2-(8-quinolinoxy)-1,3-diaza-2-phosphabicyclo-[3.3.0]- octane Ligand (QUIPHOS). Synthesis and X-ray structure of its corresponding chiral π-allyl palladium complex

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