Molecular structure of 2-allyl-4-nitrophenol, CAS Number: 19182-96-8
2-allyl-4-nitrophenol (CAS 19182-96-8)
See product citations (1)
Alternate Names:
4-nitro-2-(prop-2-en-1-yl)phenol
CAS Number:
19182-96-8
Molecular Weight:
179.17
Molecular Formula:
C9H9NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Product Citations
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
2-allyl-4-nitrophenol (ANP) is an organic compound that has been found to possess various biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. It may act to reduce the levels of reactive oxygen species and lipid peroxidation, as well as increase the levels of glutathione, an antioxidant. In addition, 2-allyl-4-nitrophenol inhibits the activity of cyclooxygenase-2, an enzyme that is involved in the production of inflammatory prostaglandins.
2-allyl-4-nitrophenol (CAS 19182-96-8) References
- New Ugi-Smiles-metathesis strategy toward the synthesis of pyrimido azepines. | El Kaïm, L., et al. 2007. J Org Chem. 72: 5835-8. PMID: 17585822
- Ugi-Smiles couplings: new entries to N-aryl carboxamide derivatives. | El Kaïm, L. and Grimaud, L. 2010. Mol Divers. 14: 855-67. PMID: 19582586
- Di-tert-butylisobutylsilyl, another useful protecting group. | Liang, H., et al. 2011. Org Lett. 13: 4120-3. PMID: 21744824
- Evidences for the key role of hydrogen bonds in nucleophilic aromatic substitution reactions. | Chéron, N., et al. 2011. Chemistry. 17: 14929-34. PMID: 22113894
- Parameters affecting the microwave-specific acceleration of a chemical reaction. | Chen, PK., et al. 2014. J Org Chem. 79: 7425-36. PMID: 25050921
- Potential antitumor agents. 58. Synthesis and structure-activity relationships of substituted xanthenone-4-acetic acids active against the colon 38 tumor in vivo. | Rewcastle, GW., et al. 1989. J Med Chem. 32: 793-9. PMID: 2704025
- Capturing Fleeting Intermediates in a Claisen Rearrangement Using Nonequilibrium Droplet Imbibition Reaction Conditions. | Sahraeian, T., et al. 2022. Anal Chem. 94: 15093-15099. PMID: 36251285
- A new synthetic approach to enantiomerically enriched dihydrobenzofurans: use of a hydrolytic kinetic resolution and an intramolecular epoxide ring opening protocol using 1-benzyloxy-2-oxiranylmethylbenzenes | Umadevi Bhoga. 2005. Tetrahedron Letters. 46: 5239-5242.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-allyl-4-nitrophenol, 250 mg | sc-274164 | 250 mg | $214.00 |