1-hydroxy-4-unsubstituted benzenoids
eMolecules 55736-04-4 | 1-(2-Chloro-6-hydroxyphenyl)ethanone | MFCD00218550 | 1g
Ambeed | 1-(2-Chloro-6-hydroxyphenyl)ethanone | 1g | 525187685 | A328859 | 55736-04-4 | MFCD00218550 | 170.590 | C8H7ClO2
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Matrix Scientific 2-HYDROXYPHENYLBORONIC ACID-5G
2-Hydroxyphenylboronic acid, -5g,C6H7BO3, MFCD01074581, mw 137.93,
Accela Chembio Inc MF: C9H10O4 | MW: 182.17 | ?96% | Flash Point: 153.1 celsius.
MF: C9H10O4 | MW: 182.17 | ?96% | Flash Point: 153.1 celsius.
eMolecules 37055-79-1 | 2-Methoxy-4-phenylphenol | Combi-Blocks | MFCD18314937 | 200.237 | C13H12O2 | 98.000 | COc1cc(ccc1O)-c1ccccc1 | 1g | 117582911
2-Methoxy-4-phenylphenol | Combi-Blocks | 37055-79-1 | MFCD18314937 | 200.237 | C13H12O2 | 98.000 | COc1cc(ccc1O)-c1ccccc1 | 1g | 117582911
Medchemexpress LLC 4-Ethylphenol-d10 | 352431-18-6 | 97.91% | 132.23 | 5 MG
4-Ethylphenol-d10 is the deuterium-labeled version of 4-Ethylphenol. 4-Ethylphenol is a volatile phenolic compound linked to off-odour in wine and can be synthesized by intestinal flora. It is converted to 4-ethylphenyl sulfate by *Lactobacillus plantarum*.
- Used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Incorporation of stable heavy isotopes (hydrogen, carbon, and other elements) into drug molecules can serve as tracers for quantitation during drug development.
- Deuteration can potentially influence the pharmacokinetic and metabolic profiles of drugs.
Medchemexpress LLC 4-Ethylphenol | 123-07-9 | 99.99% | 122.17 | 100 G
4-Ethylphenol is a volatile phenolic compound commonly associated with off-odour in wine. This phenolic compound can be synthesized by intestinal flora and is converted to 4-ethylphenyl sulfate by *Lactobacillus plantarum*.
- Causes DNA damage and induces 8-oxodG formation in calf thymus DNA in the presence of Cu (II)
- Soluble in DMSO (60 mg/mL), H2O (2.63 mg/mL)
- Available as a white to light yellow solid
- Endogenous metabolite
Medchemexpress LLC Guaiacol carbonate | 553-17-3 | MFCD00025723 | 500mg
Guaiacol Carbonate acts as an expectorant by virtue of a reflex from the stomach by way of the afferent gastric nerves to the medullary centres and thenperipherally again to the respiratory tract[1]
![eMolecules 5470-17-7 | 3-Bromo-2-chloro-5-nitropyridine | Ambeed | MFCD00233989 | 237.440 | C5H2BrClN2O2 | 98.000 | [O-][N+](=O)c1cnc(Cl)c(Br)c1 | 100g | 572824329](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000470363.jpg-250.jpg)
eMolecules 5470-17-7 | 3-Bromo-2-chloro-5-nitropyridine | Ambeed | MFCD00233989 | 237.440 | C5H2BrClN2O2 | 98.000 | [O-][N+](=O)c1cnc(Cl)c(Br)c1 | 100g | 572824329
3-Bromo-2-chloro-5-nitropyridine | Ambeed | 5470-17-7 | MFCD00233989 | 237.440 | C5H2BrClN2O2 | 98.000 | [O-][N+](=O)c1cnc(Cl)c(Br)c1 | 100g | 572824329