4780-79-4
Chemical Structure
1-Naphthalenemethanol
Synonym(s): 1-Hydroxymethylnaphthalene
- CAS No.: 4780-79-4
- Formula:C11H10O
- Molecular Weight:158.20
IUPAC Name: naphthalen-1-ylmethanol
InChIKey: PBLNHHSDYFYZNC-UHFFFAOYSA-N
SMILES: OCC1=C2C=CC=CC2=CC=C1
Biological Activity: 1-Naphthalenemethanol is a hydroxyl-substituted naphthalene derivative. 1-Naphthalenemethanol can be extracted from the root of Annona senegalensis. 1-Naphthalenemethanol is a photolysis product of 1-napthaleneacetic acid. 1-Naphthalenemethanol, together with PAPS, provides some protection against the irreversible inactivation of AST IV caused by N-OH-2AF. 1-Naphthalenemethanol can be used in antibacterial research[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
1-Naphthalenemethanol | 99.97% | 1-Naphthalenemethanol is a hydroxyl-substituted naphthalene derivative. 1-Naphthalenemethanol can be extracted from the root of Annona senegalensis. 1-Naphthalenemethanol is a photolysis product of 1-napthaleneacetic acid. 1-Naphthalenemethanol, together with PAPS, provides some protection against the irreversible inactivation of AST IV caused by N-OH-2AF. 1-Naphthalenemethanol can be used in antibacterial research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
1-Naphthalenemethanol (Standard) | 99.99% | 1-Naphthalenemethanol (Standard) is the analytical standard of 1-Naphthalenemethanol (HY-W017241). This product is intended for research and analytical applications. 1-Naphthalenemethanol is a hydroxyl-substituted naphthalene derivative. 1-Naphthalenemethanol can be extracted from the root of Annona senegalensis. 1-Naphthalenemethanol is a photolysis product of 1-napthaleneacetic acid. 1-Naphthalenemethanol, together with PAPS, provides some protection against the irreversible inactivation of AST IV caused by N-OH-2AF. 1-Naphthalenemethanol can be used in antibacterial research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Theophine Chinwuba Okoye, et al. Antimicrobial Effects of a Lipophilic Fraction and Kaurenoic Acid Isolated from the Root Bark Extracts of Annona senegalensis. Evid Based Complement Alternat Med. 2012;2012:831327. [Content Brief]
- [2]. Feng Y L, et al. UV light induced transformation of 1-methylnaphthalene in the presence of air and its implications for contaminants research. 2012.
- [3]. King RS, et al. Oxidation-dependent inactivation of aryl sulfotransferase IV by primary N-hydroxy arylamines during in vitro assays. Carcinogenesis. 1997 Apr;18(4):843-9. [Content Brief]
- [4]. Crosby D G, et al. Photodecomposition of 1-naphthaleneacetic acid[J]. Journal of Agricultural and Food Chemistry, 1969, 17(6): 1291-1293.
