586-96-9
586-96-9
Chemical Structure
Nitrosobenzene
- CAS No.: 586-96-9
- Formula:C6H5NO
- Molecular Weight:107.11
IUPAC Name: nitrosobenzene
InChIKey: NLRKCXQQSUWLCH-UHFFFAOYSA-N
SMILES: O=NC1=CC=CC=C1
Biological Activity: Nitrosobenzene is a radical scavenger that can be used to study oxidative DNA damage and the respiratory burst reaction of neutrophils induced by nitro compounds[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Nitrosobenzene | 99.32% | Nitrosobenzene is a radical scavenger that can be used to study oxidative DNA damage and the respiratory burst reaction of neutrophils induced by nitro compounds. | ||||||||||||||||||||
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2-Nitrosopyridine | 99.84% | 2-Nitrosopyridine is a nitroso compound that can be used to synthesize antibiotics. 2-Nitrosopyridine can be used as a Click or Diels-Alder derivatization reagent and an excellent dienophile. | ||||||||||||||||||||
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Benzyl alcohol | 99.99% | Benzyl alcohol is an aromatic alcohol, a colorless liquid with a mild aromatic odor. Benzyl alcohol is an inhibitor of P450 enzyme. Benzyl alcohol mediated Toll-Like Receptor 4 to reduce the inflammatory response of liver injury in mice. | ||||||||||||||||||||
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Benzyl alcohol-13C6 | 98% | Benzyl alcohol-13C6 is the 13C labeled Benzyl alcohol. | ||||||||||||||||||||
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Benzyl alcohol-13C | Benzyl alcohol-13C is the 13C labeled Benzyl alcohol (HY-B0892). Benzyl alcohol is an aromatic alcohol, a colorless liquid with a mild aromatic odor. | |||||||||||||||||||||
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Tropone (Standard) | ≥98% | Tropone (Standard) (Cycloheptatrienone (Standard)) is the analytical standard of Tropone (HY-W035904). This product is intended for research and analytical applications. Tropone (Cycloheptatrienone) is a non-benzenoid aromatic natural product that acts as a membrane reverse transporter and metal chelator. Tropone disrupts the proton motive force by affecting the transmembrane proton gradient and functions as a quorum sensing signal through LuxR-type transcriptional regulators. Tropone exhibits broad-spectrum antibiotic, anticancer, algicidal, and probiotic activities. As a virulence factor toxic to rice seedlings, Tropone promotes biofilm formation in Burkholderia plantarii and induces neurotoxicity involving mitochondrial and cytoskeletal damage, increased Ca2+ influx, and oxidative stress. Tropone is used in the study of bacterial infections. | ||||||||||||||||||||
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Phenol, potassium salt (4:1) | Phenol, potassium salt (4:1) is a metal-organic framework (MOF). | |||||||||||||||||||||
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Iodobenzene | 99.91% | Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl. | ||||||||||||||||||||
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