![4′-Methyl[1,1′-biphenyl]-4-ol](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F213385-4-methyl-11-biphenyl-4-ol.webp&w=3840&q=75)
CAS 26191-64-0: 4′-Methyl[1,1′-biphenyl]-4-ol
Formula:C13H12O
InChI:InChI=1S/C13H12O/c1-10-2-4-11(5-3-10)12-6-8-13(14)9-7-12/h2-9,14H,1H3
InChI key:InChIKey=DDZACMDGXVXOOH-UHFFFAOYSA-N
SMILES:CC1=CC=C(C=C1)C2=CC=C(O)C=C2
Synonyms:- 4'-Methylbiphenyl-4-Ol
- 4-(4-Methylphenyl)phenol
- 4-Biphenylol, 4′-methyl-
- 4-Hydroxy-4′-methyl-1,1′-biphenyl
- 4-Hydroxy-4′-methylbiphenyl
- 4′-Methyl-4-biphenylol
- 4′-Methyl-4-hydroxybiphenyl
- Phenol, p-(p-tolyl)-
- [1,1′-Biphenyl]-4-ol, 4′-methyl-
- 4′-Methyl[1,1′-biphenyl]-4-ol
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Found 4 products.
[1,1'-Biphenyl]-4-ol, 4'-methyl-
CAS:Formula:C13H12OPurity:97%Color and Shape:SolidMolecular weight:184.23384'-Methyl-1,1'-biphenyl-4-ol
CAS:4'-Methyl-1,1'-biphenyl-4-ol is a chiral compound that has been found in nature. It is a racemic mixture of two enantiomers, which means it can be separated into its two mirror images. The enantiomer with the higher reaction rate is 4'-methyl-1,1'-biphenyl-4-ol (S) and the enantiomer with the lower reaction rate is 4'-methyl-1,1'-biphenyl-4-ol (R). The two enantiomers react differently to chloride ions because one needs an extra methyl group for desymmetrization. This difference in reactivity leads to different rates of reaction and kinetic behavior. 4′-Methyl biphenylol has also been shown to have antioxidant properties by scavenging reactive oxygen species generated by thiourea.Formula:C13H12OSPurity:Min. 95%Molecular weight:216.3 g/mol4-Hydroxy-4'-methylbiphenyl
CAS:4-Hydroxy-4'-methylbiphenylFormula:C13H12OPurity:By hplc: 97% (Typical Value in Batch COA)Color and Shape: grey solidMolecular weight:184.23g/mol4'-Methyl[1,1'-biphenyl]-4-ol
CAS:Purity:95.0%Color and Shape:Solid, White powderMolecular weight:184.23800659179688