6214-09-1

Basic information

• Product Name: diphenyl piperidin-1-ylphosphonate
• Synonyms: diphenyl piperidin-1-ylphosphonate
• CAS NO: 6214-09-1
• Molecular Weight: 317.324
• Mol File: 6214-09-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: diphenyl piperidin-1-ylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diphenyl piperidin-1-ylphosphonate(6214-09-1)
• EPA Substance Registry System: diphenyl piperidin-1-ylphosphonate(6214-09-1)

Safety Data

• Hazardous Substances Data: 6214-09-1(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 26386-88-9 diphenyl phosphoryl azide 
• 838-85-7 diphenyl hydrogen phosphate 
• 2524-64-3 chlorophosphoric acid diphenyl ester 

Relevant articles and documents

When phosphoryl azide meets mechanochemistry: Clean, rapid, and efficient synthesis of phosphoryl amides under B(C6F5)3catalysis in a ball mill

We described herein the first example associated with B(C6F5)3-catalyzed preparation of phosphoryl amides under mechanochemical conditions. In this novel system, the combination of energetic reagents with an energetic mechanochemical process enabled the r

DBN hexafluorophosphate salts as convenient sulfonylating and phosphonylating agents

Air-stable N-sulfonyl and N-phosphonyl DBN hexafluorophosphate salts have been synthesised under mild conditions as sulfonylating and phosphonylating agents. These salts are highly efficient in the sulfonylation and phosphonylation of a range of N- and O-nucleophiles to generate sulfonamides, sulfonate esters, phosphoramidates and phosphonate esters in good yields.

Nucleophilic Substitution at the Tetracoordinated Phosphorus Atom. Reactivity of Amines towards Diphenyl Chlorophosphate in Acetonitrile

Tertiary alkylamines, pyridines, and imidazoles catalyze the hydrolysis of diphenylchlorophosphate (acetonitrile, 25°C) by a nucleophilic mechanism with the rate-determining attack of an amine on the substrate. Primary and secondary alkyl and arylamines f