486-79-3
486-79-3
Chemical Structure
Dipyrocetyl
- CAS No.: 486-79-3
- Formula:C11H10O6
- Molecular Weight:238.19
IUPAC Name: 2,3-diacetoxybenzoic acid
InChIKey: NYIZXMGNIUSNKL-UHFFFAOYSA-N
SMILES: O=C(O)C1=CC=CC(OC(C)=O)=C1OC(C)=O
Biological Activity: Dipyrocetyl is a Salicylic Acid (HY-B0167) derivative, exhibiting analgesic and antipyretic activity. Dipyrocetyl can be used for inflammation diseases and pain[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Dipyrocetyl | 98.16% | Dipyrocetyl is a Salicylic Acid (HY-B0167) derivative, exhibiting analgesic and antipyretic activity. Dipyrocetyl can be used for inflammation diseases and pain. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dipyrocetyl (Standard) | ≥98% | Dipyrocetyl (Standard) is the analytical standard of Dipyrocetyl. This product is intended for research and analytical applications. Dipyrocetyl is a Salicylic Acid (HY-B0167) derivative, exhibiting analgesic and antipyretic activity. Dipyrocetyl can be used for inflammation diseases and pain. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Arora R, et al. Synthesis and Antibacterial Activity of 4-Methylsalicylic Acid Derivatives and Salicylanilides. Russ J Org Chem 60, 1217-1224 (2024).
- [2]. Rosheen, et al. Salicylic Acid: Synthetic Strategies and Their Biological Activities. ChemistrySelect2023, 8, e202204614.
- [3]. Tanaka T, et al. Chemoprevention of 4-nitroquinoline 1-oxide-induced oral carcinogenesis by dietary protocatechuic acid during initiation and postinitiation phases. Cancer Res. 1994 May 1;54(9):2359-65. [Content Brief]
