63075-64-9

Basic information

• Product Name: diethyl 4-hydroxybutylphosphonate
• Synonyms: diethyl 4-hydroxybutylphosphonate
• CAS NO: 63075-64-9
• Molecular Formula: C8H19O4P
• Molecular Weight: 210.207821
• Mol File: 63075-64-9.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: diethyl 4-hydroxybutylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 4-hydroxybutylphosphonate(63075-64-9)
• EPA Substance Registry System: diethyl 4-hydroxybutylphosphonate(63075-64-9)

Safety Data

• Hazardous Substances Data: 63075-64-9(Hazardous Substances Data)

Upstream product

• 928-51-8 4-Chloro-1-butanol 
• 122-52-1 triethyl phosphite 
• 15916-48-0 diethyl but-3-en-1-ylphosphonate 
• 117345-78-5 diethyl 4-(tert-butyldimethylsilyloxy)butanephosphonate 
• 32421-69-5 diethyl 4-acetoxy-n-butylphosphonate 
• 63075-66-1 diethyl (4-bromobutyl)phosphonate 
• 38694-48-3 γ-diethoxyphosphorylbutyric acid 

Downstream Products

• 158957-14-3 3-formyl-1-propylphosphonic acid diethyl ester 
• 174538-67-1 {4-[5-(3-Benzoyl-2-methyl-isothioureido)-4-carbamoyl-[1,2,3]triazol-1-ylmethoxy]-butyl}-phosphonic acid diethyl ester 
• 174538-64-8 {4-[5-(3-Benzoyl-thioureido)-4-carbamoyl-[1,2,3]triazol-1-ylmethoxy]-butyl}-phosphonic acid diethyl ester 
• 174538-52-4 {4-[5-(3-Benzoyl-2-methyl-isothioureido)-4-carbamoyl-[1,2,3]triazol-1-yl]-butyl}-phosphonic acid diethyl ester 
• 174538-49-9 {4-[5-(3-Benzoyl-thioureido)-4-carbamoyl-[1,2,3]triazol-1-yl]-butyl}-phosphonic acid diethyl ester 

Relevant articles and documents

Synthesis and antiviral activity of new phosphonobutoxypurines

A series of new 9-(4-phosphonobutoxy)purines was synthesized and evaluated as antiviral agents. 9-(4-Phosphonobutoxy)guanine displayed potent and selective activity against HIV-1 in peripheral blood lymphocytes.

Glucose compound, medicinal composition and application thereof

The invention discloses a glucose compound, a medicinal composition and application thereof. The glucose compound or pharmaceutically acceptable salt thereof as shown in a formula I almost has no activity of inhibiting cancer cell proliferation in vitro, but has excellent anti-cancer effect and excellent inhibition effect on tumor metastasis in an in-vivo activity test, and has an excellent marketapplication prospect.

Covalent and selective immobilization of GST fusion proteins with fluorophosphonate-based probes

Using GST fusion protein tags is an attractive approach for protein immobilization. Here we report that pyrimidine-based small-molecule probes with a fluorophosphonate reactive group could specifically react with the tyrosine-111 residue of the Schistosom