CAS 705-83-9

Formel: C9H5FO2

InChl: InChI=1S/C9H5FO2/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-3,6H,(H,11,12)

InChI Key: NNOYZYGSKUOROV-UHFFFAOYSA-N

SMILES: C1=CC(=CC(=C1)F)C#CC(=O)O

3-(3-Fluorophenyl)prop-2-ynoic acid

CAS: 705-83-9

Formel: C₉H₅FO₂

Reinheit: 95%

Farbe und Form: Solid

Molekulargewicht: 164.1332

Ref: IN-DA00JSV2

3-(3-Fluorophenyl)prop-2-ynoic acid

CAS: 705-83-9

3-(3-Fluorophenyl)prop-2-ynoic acid

Formel: C₉H₅FO₂

Reinheit: 97%

Molekulargewicht: 164.133203

Ref: 54-PC100700

3-(3-Fluorophenyl)propiolic acid

CAS: 705-83-9

3-(3-Fluorophenyl)propiolic acid

Formel: C₉H₅FO₂

Reinheit: 95%

Molekulargewicht: 164.13

Ref: IN-DG01100542

3-(3-fluorophenyl)prop-2-ynoic acid

CAS: 705-83-9

Formel: C₉H₅FO₂

Reinheit: 97%

Molekulargewicht: 164.135

Ref: 10-F522361

3-(3-fluorophenyl)prop-2-ynoic acid

CAS: 705-83-9

3-(3-fluorophenyl)prop-2-ynoic acid is an organic compound that is used as a reagent in organic synthesis. It is activated with strong Lewis acids such as aluminum chloride and boron trifluoride etherate to yield the terminal alkynes. The terminal alkynes can be converted to carboxylic acids by carboxylation. 3-(3-Fluorophenyl)prop-2-ynoic acid has been shown to catalyze the reaction in which propiolic acid reacts with butyllithium, yielding methylene chloride and 1,1,1-trichloropropanol. 3-(3-Fluorophenyl)prop-2-ynoic acid also has a mononuclear structure and can be diffracted by x-rays.

Formel: C₉H₅O₂F

Reinheit: Min. 95%

Molekulargewicht: 164.13 g/mol

Ref: 3D-AAA70583