CAS 613-42-3
:p-Benzylbiphényle
- 1,1′-Biphenyl, 4-(phenylmethyl)-
- 1-Benzyl-4-phenylbenzene
- 4-Benzyl-1,1′-biphenyl
- 4-Benzylbiphenyl
- 4-Phenyldiphenylmethane
- Biphenyl, 4-benzyl-
- NSC 59812
- p-Benzylbiphenyl
- p-Biphenylylphenylmethane
- 4-(Phenylmethyl)-1,1'-biphenyl
- 4-(Phenylmethyl)-1,1′-biphenyl
4-Benzylbiphenyl
CAS :Formule :C19H16Degré de pureté :>99.0%(GC)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :244.344-Benzylbiphenyl, 98+%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C19H16Degré de pureté :98+%Couleur et forme :Crystals or powder or crystalline powder, White to pale creamMasse moléculaire :244.344-Benzylbiphenyl
CAS :Formule :C19H16Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :244.33034-BENZYLBIPHENYL
CAS :Degré de pureté :95.0%Couleur et forme :SolidMasse moléculaire :244.337005615234384-Benzylbiphenyl
CAS :4-Benzylbiphenyl is a chemical compound that belongs to the group of biphenyls. It is an isomeric form of biphenyl and has a hydroxyl group at one end. 4-Benzylbiphenyl can be synthesized from phenol and benzene via Friedel-Crafts reaction. This compound may be found in natural sources, such as plants, but its concentration is low. When exposed to neutrons, 4-benzylbiphenyl undergoes the Nitrosonium ion (NO+) reaction and yields nitrobenzene. The chloride ion present in this reaction induces constitutive activation of androstane receptor, which leads to a response pathway that regulates animal health.
Formule :C19H16Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :244.33 g/mol





