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

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

Downstream Products

• 1254692-39-1 C₁₅H₁₉BrN₃O₄PS 
• 1260249-39-5 C₂₅H₂₉BrN₃O₈P 
• 1454615-08-7 C₃₂H₄₄BrN₂O₄PS 
• 1533457-21-4 diethyl ((S)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)propanamido)(4-bromophenyl)methylphosphonate 
• 1218951-09-7 O,O-diethyl N-[2-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yloxy)benzoxyl]-1-amino-1-(4-bromophenyl)methyl phosphonate 
• 699000-93-6 diethyl (4-bromophenyl){[(E)-(1-chlorocyclohexyl)methylidene]amino}methylphosphonate 
• 699000-92-5 diethyl (4-bromophenyl){[(E)-2-chloro-2-ethyl-1-butylidene]amino}methylphosphonate 
• 699001-04-2 diethyl (E)-(4-bromophenyl){[(Z)-2-ethylbut-1-enyl]imino}methylphosphonate 
• 699001-03-1 diethyl (E)-(4-bromophenyl){[(Z)-2-methylprop-1-enyl]imino}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,

Novel coumarin-containing aminophosphonatesas antitumor agent: synthesis, cytotoxicity, DNA-Binding and apoptosis evaluation

A series of novel coumarin-containing α-aminophosphonates were synthesized and evaluated for their antitumor activities against Human colorectal (HCT-116), human nasopharyngeal carcinoma (human KB) and human lung adenocarcinoma (MGC-803) cell lines in vit

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