169565-39-3

Upstream product

• 59346-65-5 di-tert-butyl phosphorobromidate 
• 3011-34-5 4-hydroxy-3-nitrobenzaldehyde 

Downstream Products

• 169565-43-9 di-tert-butyl-4-(bromomethyl)-2-nitrophenyl phosphate 
• 169565-42-8 di-tert-butyl-4-(chloromethyl)-2-nitrophenyl phosphate 
• 169565-41-7 di-tert-butyl-4-(fluoromethyl)-2-nitrophenyl phosphate 
• 169565-40-6 di-tert-butyl-4-(hydroxymethyl)-2-nitrophenyl phosphate 

Relevant academic research and scientific papers

Substituent effects on the mechanism-based inactivation of prostatic acid phosphatase

The mechanism of the inactivation of prostatic acid phosphatase (PAP) by 4-halomethylaryl phosphates, such as 4-(fluoromethyl)phenyl phosphate (FMPP), was probed by varying the benzylic leaving group and adding a nitro group to the 2 position. These studi