AC-30580 - ethyl-bromodifluoroacetate-98 | 667-27-6
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Ethyl Bromodifluoroacetate
CAS :Formule :C4H5BrF2O2Degré de pureté :98%Couleur et forme :LiquidMasse moléculaire :202.9821Ref: IN-DA0034VW
5g21,00€10g25,00€1kg112,00€25g25,00€50g25,00€5kg362,00€100g36,00€250g54,00€500g75,00€100kgÀ demanderEthyl bromo(difluoro)acetate
CAS :Ethyl bromo(difluoro)acetateFormule :C4H5BrF2O2Degré de pureté :98%Couleur et forme : clear. colourless liquidMasse moléculaire :202.9821g/molEthyl bromodifluoroacetate
CAS :Formule :BrCF2CO2CH2CH3Degré de pureté :≥ 98.0%Couleur et forme :Clear, colourless to light yellow liquidMasse moléculaire :202.99Ethyl bromodifluoroacetate
CAS :Formule :C4H5BrF2O2Degré de pureté :98.0%Couleur et forme :LiquidMasse moléculaire :202.983Ethyl Bromodifluoroacetate
CAS :Formule :C4H5BrF2O2Degré de pureté :>98.0%(GC)Couleur et forme :Colorless to Light yellow to Light orange clear liquidMasse moléculaire :202.98Ethyl Bromodifluoroacetate
CAS :Produit contrôlé<p>Applications Ethyl bromodifluoroacetate is a fluorinated compound commonly used in Reformatsky reactions to synthesize difluoro-beta-lactams. Ethyl bromodifluoroacetate is also used as a reagent to synthesize a gallic acid derivative that exhibits plant growth promoting activity.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Konas, D., et al.: Synthesis, 2002, 2616 (2002); Negi, A., et al.: Bioorg. Med. Chem. Lett., 15, 1243 (2005); Tarui, A., et al.: Heterocycles, 73, 203 (2007)<br></p>Formule :C4H5BrF2O2Couleur et forme :NeatMasse moléculaire :202.98Ethyl bromodifluoroacetate
CAS :<p>Ethyl bromodifluoroacetate is a chemical substance that reacts with amines in the presence of copper to form a copper complex. It is used as an intermediate in the synthesis of organic compounds, such as pharmaceuticals. Ethyl bromodifluoroacetate is also used as a catalyst for cross-coupling reactions of organic molecules. This reaction requires low energy and can be performed under mild conditions. The asymmetric synthesis of ethyl bromodifluoroacetate requires few steps and only uses inexpensive starting materials. The carbonyl group is chemically stable, making it difficult to decompose or oxidize. However, hydrogen fluoride will react with ethyl bromodifluoroacetate and cause it to decompose into its elements, fluorine and carbon dioxide gas. In addition, nucleophilic attack by halides can lead to the formation of ethyl bromodifluoroacetate from other substances. Control agents are necessary</p>Formule :C4H5BrF2O2Degré de pureté :Min. 95%Couleur et forme :Colourless LiquidMasse moléculaire :202.98 g/mol








