CAS 667-27-6

Bromodifluoroacetato di etile

Descrizione:

Bromodifluoroacetato di etile è un composto chimico caratterizzato dalla sua struttura unica, che include un gruppo etile, un atomo di bromo e due atomi di fluoro legati a un gruppo acetato. Questo composto è tipicamente un liquido incolore o giallo pallido con un odore distintivo. È noto per la sua reattività, in particolare nelle reazioni di sostituzione nucleofila, a causa della presenza del gruppo carbonilico elettrofilo e degli atomi di alogeno. Bromodifluoroacetato di etile è spesso utilizzato come intermedio nella sintesi organica, in particolare nella preparazione di composti fluorurati e farmaci. È importante maneggiare questa sostanza con cautela, poiché può comportare rischi per la salute, inclusa l'irritazione della pelle, degli occhi e del sistema respiratorio. Inoltre, è consigliabile utilizzare adeguati dispositivi di protezione individuale e lavorare in un'area ben ventilata o in una cappa quando si tratta di questo composto. Le sue proprietà fisiche e chimiche, come il punto di ebollizione e la solubilità, possono variare in base alle condizioni ambientali e alle formulazioni specifiche.

Formula: C₄H₅BrF₂O₂

InChI: InChI=1/C3H5F3/c4-1-3(6)2-5/h3H,1-2H2

InChI key: InChIKey=IRSJDVYTJUCXRV-UHFFFAOYSA-N

SMILES: C(C(Br)(F)F)(OCC)=O

Sinonimi:

• 1,2,3-Trifluoropropane
• 2,2-Difluoro-2-Bromoacetate Ethyl
• 2,2-difluoro-2-Ethyl bromoacetate
• 2-Bromo-2,2-difluoroacetic acid ethyl ester
• Acetic acid, 2-bromo-2,2-difluoro-, ethyl ester
• Acetic acid, bromodifluoro-, ethyl ester
• Bromodifluoroacetic acid ethyl ester
• Ebfa
• Ethyl 2-bromo-2,2-difluoroacetate
• Ethyl bromo difluoro acetate
• Ethyl difluorobromoacetate
• Ethyl bromodifluoroacetate
• Ethyl 2,2-difluoro-2-bromoacetate
• Ethyl bromodifluoroacetate 98%
• difluorobromo ethyl acetate
• Ethylbromodifluoroacetate98%

Ethyl Bromodifluoroacetate

CAS: 667-27-6

Formula: C₄H₅BrF₂O₂

Purezza: >98.0%(GC)

Colore e forma: Colorless to Light yellow to Light orange clear liquid

Peso molecolare: 202.98

Ref: 3B-B1463

Ethyl bromo(difluoro)acetate

CAS: 667-27-6

Ethyl bromo(difluoro)acetate

Formula: C₄H₅BrF₂O₂

Purezza: 98%

Colore e forma: Colourless Liquid

Peso molecolare: 202.9821

Ref: 54-PC3162

Ethyl Bromodifluoroacetate

CAS: 667-27-6

Formula: C₄H₅BrF₂O₂

Purezza: 98%

Colore e forma: Liquid

Peso molecolare: 202.9821

Ref: IN-DA0034VW

Ethyl bromodifluoroacetate

CAS: 667-27-6

Formula: BrCF₂CO₂CH₂CH₃

Purezza: ≥ 98.0%

Colore e forma: Clear, colourless to light yellow liquid

Peso molecolare: 202.99

Ref: 7W-GK7759

Ethyl bromodifluoroacetate

CAS: 667-27-6

Formula: C₄H₅BrF₂O₂

Purezza: 98.0%

Colore e forma: Liquid

Peso molecolare: 202.983

Ref: 10-F002480

Ethyl 2-bromo-2,2-difluoroacetate

CAS: 667-27-6

Ethyl 2-bromo-2,2-difluoroacetate

Formula: C₄H₅BrF₂O₂

Purezza: 98%

Peso molecolare: 202.98

Ref: IN-DG9417

Ethyl Bromodifluoroacetate

Prodotto controllato

CAS: 667-27-6

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.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
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)

Formula: C₄H₅BrF₂O₂

Colore e forma: Neat

Peso molecolare: 202.98

Ref: TR-E678450

Ethyl Bromodifluoroacetate extrapure, 98%

CAS: 667-27-6

Formula: C₄H₅BrF₂O₂

Peso molecolare: 202.98

Ref: SR-27542

Ethyl bromodifluoroacetate

CAS: 667-27-6

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

Formula: C₄H₅BrF₂O₂

Purezza: Min. 95%

Colore e forma: Colourless Liquid

Peso molecolare: 202.98 g/mol

Ref: 3D-FE10544