AC-30580 - ethyl-bromodifluoroacetate-98 | 667-27-6
Spiacenti, non è stato trovato nessun prodotto con riferimento AC-30580, ma La invitiamo a verificare i seguenti prodotti simili:
Ethyl Bromodifluoroacetate
CAS:Formula:C4H5BrF2O2Purezza:98%Colore e forma:LiquidPeso molecolare:202.9821Ref: IN-DA0034VW
5g21,00€10g25,00€1kg112,00€25g25,00€50g25,00€5kg362,00€100g36,00€250g54,00€500g75,00€100kgPrezzo su richiestaEthyl bromo(difluoro)acetate
CAS:Ethyl bromo(difluoro)acetateFormula:C4H5BrF2O2Purezza:98%Colore e forma: clear. colourless liquidPeso molecolare:202.9821g/molEthyl bromodifluoroacetate
CAS:Formula:BrCF2CO2CH2CH3Purezza:≥ 98.0%Colore e forma:Clear, colourless to light yellow liquidPeso molecolare:202.99Ethyl bromodifluoroacetate
CAS:Formula:C4H5BrF2O2Purezza:98.0%Colore e forma:LiquidPeso molecolare:202.983Ethyl Bromodifluoroacetate
CAS:Formula:C4H5BrF2O2Purezza:>98.0%(GC)Colore e forma:Colorless to Light yellow to Light orange clear liquidPeso molecolare:202.98Ethyl Bromodifluoroacetate
CAS:Prodotto controllato<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>Formula:C4H5BrF2O2Colore e forma:NeatPeso molecolare: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>Formula:C4H5BrF2O2Purezza:Min. 95%Colore e forma:Colourless LiquidPeso molecolare:202.98 g/mol








