D151203
4,4′-Dimethylbiphenyl
97%
Synonym(s):
p,p′-Bitoluene
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About This Item
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Assay
97%
form
powder
bp
295 °C (lit.)
mp
118-120 °C (lit.)
SMILES string
Cc1ccc(cc1)-c2ccc(C)cc2
InChI
1S/C14H14/c1-11-3-7-13(8-4-11)14-9-5-12(2)6-10-14/h3-10H,1-2H3
InChI key
RZTDESRVPFKCBH-UHFFFAOYSA-N
Related Categories
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Biochemistry, 36(23), 7136-7143 (1997-06-10)
Intramolecular isotope effects associated with the benzylic hydroxylation of a series of selectively deuterated isomeric xylenes and 4,4'-dimethylbiphenyl as catalyzed by various rat liver microsomal preparations and CYP2B1 were determined. Substrate analogs in which each methyl group contained either one
The journal of physical chemistry. A, 109(44), 10168-10175 (2006-07-15)
Photooxygenation of 4,4'-dimethybiphenyl with oxygen occurs efficiently in the presence of 9-phenyl-10-methylacridinium perchlorate (AcrPh(+)ClO(4)(-)) under visible light irradiation in O(2)-saturated chloroform (CHCl(3)) to yield 4-(4'-methylphenyl)benzaldehyde as a main oxygenated product. Prolonged photoirradiation afforded the further oxygenated product, 4,4'-diformylbiphenyl. The reactive
Biochemistry, 40(29), 8597-8605 (2001-07-18)
The active site topography of rabbit CYP4B1 has been studied relative to CYP2B1 and CYP102 using a variety of aromatic probe substrates. Oxidation of the prochiral substrate cumene by CYP4B1, but not CYP2B1 or CYP102, resulted in the formation of
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