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 1140716, Rietz E, "Diacidylpyrocatechin-ortho-carboxylic-acid Compound.", issued 25 May 1915, assigned to Synthetic Patents Company, Inc.
Budavari S (1989). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th, centennial ed.). Rahway, N.J., U.S.A.: Merck. p. 3358. ISBN 978-0-911910-28-5.

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[1] US 1140716, Rietz E, "Diacidylpyrocatechin-ortho-carboxylic-acid Compound.", issued 25 May 1915, assigned to Synthetic Patents Company, Inc.

[2] Budavari S (1989). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th, centennial ed.). Rahway, N.J., U.S.A.: Merck. p. 3358. ISBN 978-0-911910-28-5.

Non-steroidal 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 Bufexamac Bumadizone Diclofenac Difenpiramide Etodolac Felbinac Fenclozic acid Fentiazac Indometacin Indometacin farnesil Isoxepac Ketorolac Lonazolac Mofezolac Oxametacin Prodolic acid Proglumetacin Sulindac Tiopinac Tolmetin Zomepirac^†
oxicams	Ampiroxicam Droxicam Isoxicam Lornoxicam Meloxicam Piroxicam Pivoxicam Tenoxicam
propionic acid derivatives (profens)	Alminoprofen Benoxaprofen^† Carprofen^‡ Dexibuprofen Dexketoprofen Fenbufen Fenoprofen Flunoxaprofen Flurbiprofen Ibuprofen^# Ibuproxam Indoprofen^† Ketoprofen Loxoprofen Miroprofen Naproxen Oxaprozin Piketoprofen Pirprofen Suprofen Tarenflurbil Tepoxalin^‡ Tiaprofenic acid Vedaprofen^‡ Zaltoprofen COX-inhibiting nitric oxide donator: Naproxcinod
n-arylanthranilic acids (fenamates)	Azapropazone Clonixin Etofenamate Floctafenine Flufenamic acid Flunixin Flutiazin Glafenine^† Meclofenamic acid Mefenamic acid Morniflumate Niflumic acid Tolfenamic acid
COX-2 inhibitors (coxibs)	Apricoxib Celecoxib (+tramadol) 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
NSAID combinations	Ibuprofen/famotidine Ibuprofen/hydrocodone Ibuprofen/oxycodone Ibuprofen/paracetamol Meloxicam/bupivacaine Naproxen/diphenhydramine Naproxen/esomeprazole
Key: underline indicates initially developed first-in-class compound of specific group; ^#WHO-Essential Medicines; ^†withdrawn drugs; ^‡veterinary use.
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