1235612-77-7

Basic information

• Product Name: C₁₅H₁₇ClNO₄P
• Synonyms: C₁₅H₁₇ClNO₄P
• CAS NO: 1235612-77-7
• Molecular Weight: 341.731
• Mol File: 1235612-77-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₇ClNO₄P(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₇ClNO₄P(1235612-77-7)
• EPA Substance Registry System: C₁₅H₁₇ClNO₄P(1235612-77-7)

Safety Data

• Hazardous Substances Data: 1235612-77-7(Hazardous Substances Data)

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 106-47-8 4-chloro-aniline 
• 121-45-9 phosphorous acid trimethyl ester 

Relevant articles and documents

One-pot synthesis of α-Aminophosphonates catalyzed by boric acid at room temperature

A simple, efficient, and general method has been developed for the one-pot, three-component synthesis of α-aminophosphonates from a condensation reaction of trimethyl phosphite, aldehydes, and amines in the presence of catalytic amount of boric acid (10 mol%) under solvent-free conditions. Thus α-aminophosphonates were synthesized relatively quickly in good yields at room temperature

Cobalt(II) chloride accelerated one-pot three-component synthesis of α-aminophosphonates at room temperature

A simple, efficient, and general method has been developed for the one-pot, three-component synthesis of α-aminophosphonates from condensation reaction of trimethyl phosphite, aryl aldehydes and aryl amines in the presence of CoCl2·6H2O under solvent-free conditions. Thus α-aminophosphonates were synthesized relatively quickly in good yields at room temperature.