CAS 947-84-2
:1-Biphenyl-2-carbonsäure
- 1-Biphenyl-2-carboxylic acid
- 2-Biphenyl carboxylic acid
- 2-Carboxybiphenyl
- 2-Phenylbenzoic acid
- 4′-Isopropylcarbonylbiphenyl-2-carboxylic acid
- Biphenyl-2-Carboxylate
- Biphenyl-2-Carboxylic Acid
- Diphenyl-2-carboxylic acid
- NSC 76051
- [1,1′-Biphenyl]-2-carboxylic acid
- o-Phenylbenzoic acid
- Weitere Synonyme anzeigen
Biphenyl-2-carboxylic Acid
CAS:Formel:C13H10O2Reinheit:>98.0%(GC)(T)Farbe und Form:White to Light yellow to Light orange powder to lumpMolekulargewicht:198.22Biphenyl-2-carboxylic acid, 98%
CAS:It is used as a pharmaceutical intermediate. he reaction of 2?-substituted biphenyl-2-carboxylic acids (where the 2?-substituent is H, CO2H, NO2, Cl, OMe, or CO2Me) with lead tetra-acetate in refluxing benzene solution, under a nitrogen atmosphere, affords 3,4-benzocoumarin as a major organic produc
Formel:C13H10O2Reinheit:98%Farbe und Form:White to pale cream, Crystals or powder or crystalline powderMolekulargewicht:198.22[1,1'-Biphenyl]-2-carboxylic acid
CAS:Formel:C13H10O2Reinheit:97%Farbe und Form:SolidMolekulargewicht:198.21732-Biphenylcarboxylic acid
CAS:2-Biphenylcarboxylic acid (2BCA) is a metabolite of biphenyl. The hydroxyl group on 2BCA binds to the receptor, producing an antihypertensive effect. It has been shown to be effective in the treatment of metabolic disorders and diseases such as diabetes mellitus, hypertension, and heart disease. 2BCA is also effective in the treatment of tumors because it inhibits tumor cell growth by binding to fatty acids. This drug forms hydrogen bonds with other molecules due to its hydroxyl group and can be synthesized through a Suzuki coupling reaction.
2BCA has been found to have an inhibitory effect on prostaglandin synthesis through the p2 receptor activity.Formel:C13H10O2Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:198.22 g/mol2-Biphenylcarboxylic acid
CAS:Formel:C13H10O2Reinheit:97%Farbe und Form:Solid, Beige powderMolekulargewicht:198.221






