1038997-74-8

Basic information

• Product Name: C₇H₈O₃S*C₁₅H₂₆NO₃P
• CAS NO: 1038997-74-8
• Molecular Weight: 471.555
• Mol File: 1038997-74-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₇H₈O₃S*C₁₅H₂₆NO₃P(CAS DataBase Reference)
• NIST Chemistry Reference: C₇H₈O₃S*C₁₅H₂₆NO₃P(1038997-74-8)
• EPA Substance Registry System: C₇H₈O₃S*C₁₅H₂₆NO₃P(1038997-74-8)

Safety Data

• Hazardous Substances Data: 1038997-74-8(Hazardous Substances Data)

Upstream product

• 1038997-69-1 C₂₂H₃₀NO₃P 
• 104-15-4 toluene-4-sulfonic acid 
• 100-52-7 benzaldehyde 
• 92-29-5 hydrobenzamide 
• 92-29-5 (E,E)-1,3,5-triphenyl-2,4-diazapenta-1,4-diene 

Downstream Products

• 1300734-65-9 dibutyl((5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-arboxamido)(phenyl)methyl)phosphonate 
• 1300734-70-6 dibutyl((5-chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamido)(phenyl)methyl)phosphonate 
• 1300734-60-4 dibutyl ((5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxamido)-(phenyl)methyl)phosphonate 
• 1192761-60-6 O,O'-di-n-butyl isothiocyanato(phenyl)methylphosphonate 
• 1352612-49-7 dibutyl (3-(6-fluorobenzo[d]thiazol-2-yl)thioureido)(phenyl)methylphosphonate 
• 1352612-53-3 dibutyl (3-(4-methylbenzo[d]thiazol-2-yl)thioureido)(phenyl)methylphosphonate 
• 1352612-57-7 dibutyl (3-(6-methoxybenzo[d]thiazol-2-yl)thioureido)(phenyl)methylphosphonate 
• 1352612-61-3 dibutyl (3-(6-ethoxybenzo[d]thiazol-2-yl)thioureido)(phenyl)methylphosphonate 
• 1347739-97-2 O,O-di-n-butyl [2-(4,6-dimethoxypyrimidin-2-yloxy)phenoxyamino](phenyl)methylphosphonate 

Relevant articles and documents

Synthesis and bioactivities of α-aminophosphonate derivatives containing benzothiazole and thiourea moieties

The synthesis of a series of novel α-aminophosphonate derivatives containing benzothiazole and thiourea moieties from substituted 2-aminobenzothiazoles and synthetic intermediates O,O'-dialkylisothiocyanat- (phenyl)methylphosphonates under microwave irradiation has been demonstrated. Several salient features, such as good to excellent yields, shorter reaction times, milder reaction conditions, and simple purification procedures, make the present synthetic protocol highly attractive to access the title compounds. Bioassays indicated that most of the compounds possessed broad-spectrum insecticidal and antiviral activities against Tobacco Mosaic Virus (TMV) in vivo. Interestingly, in comparison with control insecticide Avermectin, two compounds displayed remarkably high in vitro insecticidal activities against Plutella xylostella. Furthermore, according to the results from preliminary bioassay, all were associated with moderate to good anti-TMV activities. [Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental resource: Tables S1-S4. Figures S1-S52.] Copyright Taylor and Francis Group, LLC.

Synthesis and biological evaluation of novel phosphonates derivatives of as potential antitumor agents

A series of dialkyl [2-(4,6-dimethoxypyrimidin-2-yloxy)benzamido](aryl) methylphosphonates derivatives were designed and synthesized. All the new compounds were identified by elemental analysis, IR, 1H NMR, 31P NMR, and MS. Their antitumor activity against KB and CNE1 cells was examined. Some of the compounds showed potential antitumor activity, which provided some hints for further study of structure modification. In particular, the compounds 6i and 6j displayed more potent cytotoxic activities against KB in comparison with 5-FU. Copyright Taylor & Francis Group, LLC.