Aromatic hydrocarbons
![Aobchem 1-[1 1 -Biphenyl]-4-ylethanone oxime | ≥95% | CAS 75408-89-8 | C14H13NO | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000862654.png-250.jpg)
Aobchem 1-[1 1 -Biphenyl]-4-ylethanone oxime | ≥95% | CAS 75408-89-8 | C14H13NO | 1g
1-[1 1 -Biphenyl]-4-ylethanone oxime | ≥95% | CAS 75408-89-8 | C14H13NO | 1g
Aobchem 1 3-Dichloro-2-ethylbenzene | ≥95% | CAS 33407-02-2 | C8H8Cl2 | 1g
1 3-Dichloro-2-ethylbenzene | ≥95% | CAS 33407-02-2 | C8H8Cl2 | 1g
![Aobchem 2 -Bromo-[1 1 -biphenyl]-2-carboxylic acid | ≥97% | CAS 69200-16-4 | C13H9BrO2 | 500mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000902955.png-250.jpg)
Aobchem 2 -Bromo-[1 1 -biphenyl]-2-carboxylic acid | ≥97% | CAS 69200-16-4 | C13H9BrO2 | 500mg
2 -Bromo-[1 1 -biphenyl]-2-carboxylic acid | ≥97% | CAS 69200-16-4 | C13H9BrO2 | 500mg
Aobchem 1-(3 -Chloro-[1 1 -biphenyl]-3-yl)-2 2 2-trifluoroethanone | 97% | C14H8ClF3O | 250mg
1-(3 -Chloro-[1 1 -biphenyl]-3-yl)-2 2 2-trifluoroethanone | 97% | C14H8ClF3O | 250mg
Aobchem (2-Ethoxy-[1 1 -biphenyl]-3-yl)(methyl)sulfane | 95% | CAS 2807456-33-1 | C15H16OS | 1g
(2-Ethoxy-[1 1 -biphenyl]-3-yl)(methyl)sulfane | 95% | CAS 2807456-33-1 | C15H16OS | 1g
Aobchem 2-Ethoxy-[1 1 -biphenyl]-3-carboxylic acid | 95% | CAS 810683-08-0 | C15H14O3 | 250mg
2-Ethoxy-[1 1 -biphenyl]-3-carboxylic acid | 95% | CAS 810683-08-0 | C15H14O3 | 250mg
Aobchem 2 4-Difluoro-biphenyl-5-ylboronic acid | 95% | C12H9BF2O2 | 1g
2 4-Difluoro-biphenyl-5-ylboronic acid | 95% | C12H9BF2O2 | 1g
Aobchem 3-Methoxy- -(1-methylbutyl)benzenemethanol | 95% | CAS 1341083-17-7 | C13H20O2 | 250mg
3-Methoxy- -(1-methylbutyl)benzenemethanol | 95% | CAS 1341083-17-7 | C13H20O2 | 250mg
Apexbio Technology LLC 4-METHYLBIPHENYL-500MG
4-Methylbiphenyl (CAS No 644-08-6) is a compound commonly studied in biomedical research due to its potential role in modulating biochemical pathways Originating from the biphenyl chemical family it is often investigated for its interactions with specific cellular targets though its precise mechanisms of action remain under exploration In vitro studies frequently report activity in the nanomolar to low micromolar range indicating its relevance in various experimental settings It is commonly utilized in cell models to assess cellular responses and in animal studies to evaluate pharmacokinetic properties Additionally 4-Methylbiphenyl is used in drug screening programs to identify its potential as a therapeutic candidate Experimental concentrations typically depend on the specific research design allowing flexibility in various investigative approaches