CAS 25294-65-9

Fórmula: C9H5BrO2

InChI: InChI=1S/C9H5BrO2/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-2,4-5H,(H,11,12)

Clave InChI: GZFOMZGALYVQDX-UHFFFAOYSA-N

SMILES: C1=CC(=CC=C1C#CC(=O)O)Br

3-(4-Bromophenyl)propiolic Acid

CAS: 25294-65-9

Fórmula: C₉H₅BrO₂

Pureza: >98.0%(GC)

Forma y color: White to Light yellow to Light orange powder to crystal

Peso molecular: 225.04

Ref: 3B-B5243

3-(4-Bromophenyl)prop-2-ynoic acid

CAS: 25294-65-9

3-(4-Bromophenyl)prop-2-ynoic acid

Fórmula: C₉H₅BrO₂

Pureza: 97%

Peso molecular: 225.04

Ref: 54-OR1034924

3-(4-Bromophenyl)Propiolic Acid

CAS: 25294-65-9

Fórmula: C₉H₅BrO₂

Pureza: 98%

Forma y color: Solid

Peso molecular: 225.0388

Ref: IN-DA00IMDJ

3-(4-Bromophenyl)prop-2-ynoic acid

CAS: 25294-65-9

Pureza: 97%

Peso molecular: 225.0410004

Ref: 10-F718308

3-(4-Bromophenyl)propiolic Acid

CAS: 25294-65-9

3-(4-Bromophenyl)propiolic acid is an alkynyl compound that can be synthesized by the catalyzed cross-coupling of triarylbismuth with aryl bromides. This reaction requires a catalyst and is carried out in the presence of a base, such as potassium carbonate. The reaction proceeds rapidly at room temperature and can be performed using either an organic or inorganic solvent. The product is obtained in high yield, but it must be purified to remove any residual starting materials and byproducts. 3-(4-Bromophenyl)propiolic acid has a carboxylic functional group that can undergo further reactions to form other compounds, such as cross-coupling reactions with alkenes or carboxylic acids.

Fórmula: C₉H₅BrO₂

Pureza: Min. 95%

Peso molecular: 225.04 g/mol

Ref: 3D-ABA29465