1-hydroxy-4-unsubstituted benzenoids
Aobchem 3-Ethylphenol | ≥97% | CAS 620-17-7 | C8H10O | 10g
3-Ethylphenol | ≥97% | CAS 620-17-7 | C8H10O | 10g
Aobchem 2-Iodo-6-nitrophenol | ≥95% | CAS 13073-26-2 | C6H4INO3 | 500mg
2-Iodo-6-nitrophenol | ≥95% | CAS 13073-26-2 | C6H4INO3 | 500mg
Aobchem 2-Fluoro-3-isopropoxyphenol | ≥95% | CAS 1243452-19-8 | C9H11FO2 | 5g
2-Fluoro-3-isopropoxyphenol | ≥95% | CAS 1243452-19-8 | C9H11FO2 | 5g
Aobchem 4-Bromo-2-ethylphenol | ≥95% | CAS 18980-21-7 | C8H9BrO | 25g
4-Bromo-2-ethylphenol | ≥95% | CAS 18980-21-7 | C8H9BrO | 25g
Aobchem 2-Ethoxy-5-ethylphenol | 95% | CAS 1466788-20-4 | C10H14O2 | 250mg
2-Ethoxy-5-ethylphenol | 95% | CAS 1466788-20-4 | C10H14O2 | 250mg
Aobchem 6-Bromo-3-methyl-2-nitrophenol | ≥95% | CAS 1195533-07-3 | C7H6BrNO3 | 250mg
6-Bromo-3-methyl-2-nitrophenol | ≥95% | CAS 1195533-07-3 | C7H6BrNO3 | 250mg
Medchemexpress LLC 1-Indanone (α-Hydrindone) | 83-33-0 | 132.16 | 25 G
1-Indanone is a biochemical reagent that can be utilized as a biological material or organic compound for life science-related research. It is an oxidation product and a component found in fuels, solvents, and varnishes. Additionally, it plays a role in steroid hormone biosynthesis and arachidonic acid metabolism pathways.
- Used as a biochemical reagent for life science research
- Functions as a biological material or organic compound
- Acts as an oxidation product
- A component in fuels, solvents, and varnishes
- Involved in steroid hormone biosynthesis and arachidonic acid metabolism pathways
Aobchem 3-Isopropoxyphenol | ≥95% | CAS 68792-12-1 | C9H12O2 | 5g
3-Isopropoxyphenol | ≥95% | CAS 68792-12-1 | C9H12O2 | 5g
Aobchem 4-Bromo-2-ethylphenol | ≥95% | CAS 18980-21-7 | C8H9BrO | 250mg
4-Bromo-2-ethylphenol | ≥95% | CAS 18980-21-7 | C8H9BrO | 250mg
Sigma Aldrich Fine Chemicals Biosciences (R)-(-)-Phenylephrine hydrochloride powder | 61-76-7 | MFCD00012605 | 50G
(R)-(-)-Phenylephrine hydrochloride powder | Mol Wt: 203.67 | 61-76-7 | MFCD00012605 | 50G
Matrix Scientific 2-HYDROXYPHENYLBORONIC ACID-5G
2-Hydroxyphenylboronic acid, -5g,C6H7BO3, MFCD01074581, mw 137.93,
eMolecules 79370-78-8 | 5-Hydroxyisophthalonitrile | MFCD11865326 | 1g
Ambeed | 5-Hydroxyisophthalonitrile | 1g | 525004633 | A112341 | 79370-78-8 | MFCD11865326 | 144.133 | C8H4N2O
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool<|a>
Medchemexpress LLC 4-Ethylphenol | 123-07-9 | 99.99% | 122.17 | 1 ML
4-Ethylphenol is an endogenous metabolite and volatile phenolic compound. It is associated with off-odour in wine and can be synthesized by intestinal flora, where it is converted to 4-ethylphenyl sulfate. This compound causes DNA damage and induces 8-oxodG formation, and it also reduces oligodendrocyte maturation and myelination, increasing anxiety-like behavior in mouse models.
- Purity: 99.99%
- CAS number: 123-07-9
- Molecular weight: 122.17
- Formula: C8H10O
- Appearance: Solid, white to light yellow
- Structure classification: Phenols, Monophenols
- Solubility: DMSO (60 mg/mL), H2O (2.63 mg/mL)
- Applications: For research use only
- Biological activity includes DNA damage, reduced oligodendrocyte maturation, and increased anxiety-like behavior
Sigma Aldrich Fine Chemicals Biosciences (R)-(−)-Phenylephrine Hydrochloride | 61-76-7 | MFCD00012605 | 10g
(R)-(−)-Phenylephrine Hydrochloride | Mol Wt: 203.67 | 61-76-7 | MFCD00012605 | 10g
Apexbio Technology LLC 4-Ethylphenol 123-07-9 200mg
4-Ethylphenol (CAS 123-07-9) is a volatile phenolic compound predominantly produced through the microbial decarboxylation and reduction of p-coumaric acid during fermentation and other metabolic processes It is frequently utilized to investigate the microbial enzymatic pathways underlying aromatic compound metabolism In biomedical research 4-ethylphenol serves as a model molecule for studying the interplay between microbial metabolites and host metabolic networks as well as for the identification of microbial biomarkers in health and disease Its applications extend to experiments addressing the dynamics of microbial communities and host-microbe interactions