3D-FD160933 - di-tert-butyl-chlorophosphate | 56119-60-9
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Bis(2,6-dimethylphenyl) Chlorophosphate
CAS:Formula:C16H18ClO3PPurity:>93.0%(T)Color and Shape:White to Light yellow to Light red powder to crystalMolecular weight:324.74Diphenyl Chlorophosphate
CAS:Formula:C12H10ClO3PPurity:>95.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:268.63Diethyl Chlorophosphate
CAS:Formula:C4H10ClO3PPurity:>97.0%(T)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:172.54Dimethyl Chlorophosphate
CAS:Formula:C2H6ClO3PPurity:>98.0%(GC)(T)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:144.49Diphenyl Chlorophosphate
CAS:Formula:C12H10ClO3PPurity:95%Color and Shape:LiquidMolecular weight:268.6328Bis(2,4-dichlorophenyl) Chlorophosphate (>80%)
CAS:<p>Applications A phosphate catalyst used in the direct conversion of alcohols to azides via activation. It also acts as a coupling agent in the synthesis of oligonucleotide phosphorodithioates.<br>References Yu, C. et al.: Org. Lett., 2, 1959 (2000); Kamaike, K. et al.: Nucleic Acids. Res. Supp., 3, 93 (2003);<br></p>Formula:C12H6Cl5O3PPurity:>80%Color and Shape:NeatMolecular weight:406.41Bis(2,4-dichlorophenyl) chlorophosphate
CAS:<p>Bis(2,4-dichlorophenyl) chlorophosphate is a surfactant that is used in the production of ammonium hexafluorophosphate. It is also used in the manufacture of alcohols and deionized water. Bis(2,4-dichlorophenyl) chlorophosphate has been shown to be an effective reagent for the synthesis of fluorophosphates.</p>Formula:C12H6Cl5O3PPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:406.41 g/molDiphenyl chlorophosphate
CAS:<p>Diphenyl chlorophosphate is a reactive molecule that is classified as an organic compound. It has been synthesized in vitro by reacting sodium carbonate with p-hydroxybenzoic acid and trifluoroacetic acid. The synthesis of this compound was successful because the hydroxyl group on p-hydroxybenzoic acid reacted with the amide group on sodium carbonate to form an amide linkage. This reaction also created an alkanoic acid, which was hydrolyzed to form an ester linkage between the two molecules. Diphenyl chlorophosphate has been shown to bind to receptor molecules and inhibit their activity, which may be due to its ability to react with other molecules in order to produce a new product.</p>Formula:C12H10ClO3PPurity:Min. 99.0 Area-%Color and Shape:Clear LiquidMolecular weight:268.63 g/molDiphenyl chlorophosphate
CAS:Formula:C12H10ClO3PPurity:95%Color and Shape:ClearMolecular weight:268.63Diethyl chlorophosphate, 97+%
CAS:<p>A phosphorous halide used for biochemical research. Also used as an intermediate in organic synthesis. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aes</p>Formula:C4H10ClO3PPurity:97+%Color and Shape:Clear colorless, LiquidMolecular weight:172.54Bis(2,4-dichlorophenyl) chlorophosphate, tech grade
CAS:Formula:C12H6Cl5O3PPurity:95%Color and Shape:SolidMolecular weight:406.4130Bis(butoxyethyl)chlorophosphate
CAS:Controlled Product<p>Applications Bis(butoxyethyl)chlorophosphate is an intermediate in synthesizing Bis(2-butoxyethyl) 2-Hydroxyethyl Phosphate Triester (B415190), a metabolite of Tris(2-butyloxyethyl)phosphate (T875030), which is an organophosphate, that can be used in the preparation of flame retardant, such as viscose fiber.<br>References Wang, Y., et al.: Fangzhi Xuebao, 33, 16 (2012); Xiaoshan, L. et al.: Aquatic Toxicology, 114, 173 (2012)<br></p>Formula:C12H26ClO5PColor and Shape:NeatMolecular weight:316.76Bis(butoxyethyl)chlorophosphate-d8
CAS:Controlled ProductFormula:C12D8H18ClO5PColor and Shape:NeatMolecular weight:324.808Diethyl Chlorophosphate-d10
CAS:Controlled Product<p>Applications Diethyl Chlorophosphate-d10 is an intermediate in the synthesis of Chlorpyrifos Oxon-d10 (C425322), which is an isotope labeled analogue of Chlorpyrifos Oxon (C425320). a metabolite of Chlorpyrifos (C425300) in human.<br>References Atterberry, T., et al.: Toxicol. Appl. Pharmacol., 147, 411 (1997), Karanth, S., et al.: Toxicol. Sci., 58, 282 (2000), Barter, Z., et al.: Drug Metab. Dispos., 36, 2405 (2008),<br></p>Formula:C4D10ClO3PColor and Shape:NeatMolecular weight:182.61







