| Weight | 168.239 g/mol |
|---|---|
| Formula | C13H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-Methylbiphenyl (644-08-6)
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- Vibrational spectroscopic, molecular structure, first hyperpolarizability and NBO studies of 4'-methylbiphenyl-2-carbonitrile. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- THERMOCHEMICAL AND THEORETICAL STUDIES OF 4-METHYLBIPHENYL, 4,4'-DIMETHYLBIPHENYL, 4,4'-DIMETHYL-2,2'-BIPYRIDINE (Journal of the Chemical Society, Faraday Transactions, 1997)
- Molecular structure, spectroscopic (FT-IR, FT-Raman, 13C and 1H NMR, UV), polarizability and first-order hyperpolarizability, HOMO and LUMO analysis of 4'-methylbiphenyl-2-carbonitrile. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- Effects of SiO2/Al2O3, MgO modification and hydrothermal treatment on the catalytic activity of HZSM-5 zeolites in the methylation of 4-methylbiphenyl with methanol (Applied Catalysis A-general, 2004)
- Nickel-Catalyzed Cross-Coupling Reaction of Aryl Halides in Pyridine. A Practical Synthesis of 4-Methylbiphenyl-2-carbonitrile As a Key Intermediate of Angiotensine II Receptor Antagonists (Synlett, 1994)
- Shape-selective synthesis of 4,4-dimethylbiphenyl. 1. Methylation of 4-methylbiphenyl over modified zeolite catalysts (Catalysis Letters, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=C(C=C1)C2=CC=CC=C2
-
InChIKeyZZLCFHIKESPLTH-UHFFFAOYSA-N
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