Dipyrocetyl

Dipyrocetyl
Clinical data
Trade names	Movirene; Artromialgina
Other names	2,3-Bis(acetyloxy)benzoic acid; o-Pyrocatechuic acid diacetate; Diacetylpyrocatechol-3-carboxylic acid
ATC code	N02BA09 (WHO) ;
Identifiers
	IUPAC name 2,3-Diacetoxybenzoic acid;
CAS Number	486-79-3;
PubChem CID	68093;
ChemSpider	61404;
UNII	EF5UVE254C;
ChEMBL	ChEMBL1451173;
CompTox Dashboard (EPA)	DTXSID9045976 ;
ECHA InfoCard	100.006.947
Chemical and physical data
Formula	C11H10O6
Molar mass	238.195 g·mol−1
3D model (JSmol)	Interactive image;
Melting point	148 to 150 °C (298 to 302 °F) [1]
Solubility in water	Insoluble mg/mL (20 °C)
	SMILES O=C(Oc1cccc(c1OC(=O)C)C(=O)O)C;
	InChI InChI=1S/C11H10O6/c1-6(12)16-9-5-3-4-8(11(14)15)10(9)17-7(2)13/h3-5H,1-2H3,(H,14,15); Key:NYIZXMGNIUSNKL-UHFFFAOYSA-N;

Dipyrocetyl is a pharmaceutical drug used as an analgesic and antipyretic.[2]

References

US patent 1140716, Rietz
Merck Index, 11th Edition, 3358

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[1] US patent 1140716, Rietz

[2] Merck Index, 11th Edition, 3358

Nonsteroidal anti-inflammatory drugs (NSAIDs) (primarily M01A and M02A, also N02BA)
Pyrazolones / Pyrazolidines	Aminophenazone Ampyrone Azapropazone Clofezone Difenamizole Famprofazone Feprazone Kebuzone Metamizole Mofebutazone Morazone Nifenazone Oxyphenbutazone Phenazone Phenylbutazone Propyphenazone Sulfinpyrazone Suxibuzone^‡
Salicylates	Aspirin (acetylsalicylic acid)^# Aloxiprin Benorylate Carbasalate calcium Diflunisal Dipyrocetyl Ethenzamide Guacetisal Magnesium salicylate Methyl salicylate Salsalate Salicin Salicylamide Salicylic acid (salicylate) Sodium salicylate
Acetic acid derivatives and related substances	Aceclofenac Acemetacin Alclofenac Amfenac Bendazac Bromfenac Bumadizone Bufexamac Diclofenac Difenpiramide Etodolac Felbinac Fenclozic acid Fentiazac Indometacin Indometacin farnesil Isoxepac Ketorolac Lonazolac Oxametacin Prodolic acid Proglumetacin Sulindac Tiopinac Tolmetin Zomepirac^†
Oxicams	Ampiroxicam Droxicam Isoxicam Lornoxicam Meloxicam Piroxicam Tenoxicam
Propionic acid derivatives (profens)	Alminoprofen Benoxaprofen^† Carprofen^‡ Dexibuprofen Dexketoprofen Fenbufen Fenoprofen Flunoxaprofen Flurbiprofen Ibuprofen^# Ibuproxam Indoprofen^† Ketoprofen Loxoprofen Miroprofen Naproxen Oxaprozin Pirprofen Suprofen Tarenflurbil Tepoxalin^‡ Tiaprofenic acid Vedaprofen^‡ Zaltoprofen COX-inhibiting nitric oxide donator: Naproxcinod
N-Arylanthranilic acids (fenamates)	Azapropazone Clonixin Etofenamate Flufenamic acid Flunixin Meclofenamic acid Mefenamic acid Morniflumate Niflumic acid Tolfenamic acid Flutiazin
Coxibs	Apricoxib Celecoxib Cimicoxib^‡ Deracoxib^‡ Etoricoxib Firocoxib^‡ Lumiracoxib^† Mavacoxib^‡ Parecoxib Robenacoxib^‡ Rofecoxib^† Valdecoxib^†
Other	Aminopropionitrile Benzydamine Chondroitin sulfate Diacerein Fluproquazone Glucosamine Glycosaminoglycan Hyperforin Nabumetone Nimesulide Oxaceprol Proquazone Superoxide dismutase/Orgotein Tenidap
Combinations	Ibuprofen/paracetamol Meloxicam/bupivacaine
Items listed in bold indicate initially developed compounds of specific groups. ^#WHO-EM ^†Withdrawn drugs. ^‡Veterinary use medications.