189180-13-0

Basic information

• Product Name: Phosphonic acid, [amino(4-bromophenyl)methyl]-, diethyl ester
• CAS NO: 189180-13-0
• Molecular Formula: C11H17BrNO3P
• Molecular Weight: 322.139
• Mol File: 189180-13-0.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [amino(4-bromophenyl)methyl]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [amino(4-bromophenyl)methyl]-, diethyl ester(189180-13-0)
• EPA Substance Registry System: Phosphonic acid, [amino(4-bromophenyl)methyl]-, diethyl ester(189180-13-0)

Safety Data

• Hazardous Substances Data: 189180-13-0(Hazardous Substances Data)

Upstream product

• 24523-45-3 bis-(4-bromo-benzylidene)-hydrazine 
• 762-04-9 phosphonic acid diethyl ester 
• 871315-33-2 ((4-Bromo-phenyl)-{[1-(4-bromo-phenyl)-meth-(E)-ylidene]-amino}-methyl)-phosphonic acid diethyl ester 
• 1122-91-4 4-bromo-benzaldehyde 
• 20641-24-1 diethyl ((4-bromophenyl)(hydroxy)methyl)phosphonate 
• 335197-65-4 [Azido-(4-bromo-phenyl)-methyl]-phosphonic acid diethyl ester 
• 762-04-9 Diethyl phosphonate 

Downstream Products

• 1254692-39-1 C₁₅H₁₉BrN₃O₄PS 
• 1260249-39-5 C₂₅H₂₉BrN₃O₈P 
• 1454615-08-7 C₃₂H₄₄BrN₂O₄PS 
• 699000-79-8 diethyl (4-bromophenyl){[(E)-2-ethyl-1-butylidene]amino}methylphosphonate 

Relevant articles and documents

Parietic acid aminophosphonic acid ester derivative and its synthetic method and application

The invention discloses a series of rhein aminophosphonate derivatives, and a synthetic method and applications thereof. The synthetic method of the rhein aminophosphonate derivatives comprises: taking rhein and an alpha-aminophosphonate as raw materials,

Synthesis of derivatives of artesunate α-aminophosphonate and their antimicrobial activities

Thirteen α-aminophosphonate derivatives with artesunate were synthesized by introducing bioactive α-aminophosphonate combination with artesunate in this work. The reaction were easily carried out at normal pressure, low temperature and without any catalys

Synthesis and antitumor activities of novel rhein α-aminophosphonates conjugates

Several rhein α-aminophosphonates conjugates (5a-5q) were synthesized and evaluated for in vitro cytotoxicity against HepG-2, CNE, Spca-2, Hela and Hct-116 cell lines. Some compounds showed relatively high cytotoxicity. Especially, compound 5i exhibited t