| Weight | 223.272 g/mol |
|---|---|
| Formula | C12H17NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Bucetin
beta-hydroxybutyric acid-p-phenetidide · NHB-PPT · N-(beta-hydroxybutyryl)-p-phenetidine
156674-11-2, 156674-10-1, 1083-57-4
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- Mechanism of metabolic activation of the analgetic bucetin to bacterial mutagens by hamster liver microsomes. (Chemical & Pharmaceutical Bulletin, 1985)
- Carcinogenicity of Bucetin in (C57BL/6 C3H)F1 Mice (Journal of the National Cancer Institute, 1987)
- Drug Absorption, Metabolism, and Excretion. II. Metabolism of Bucetin (-Hydroxybutyro-p-phenetidide) in Rabbits (Chemical & Pharmaceutical Bulletin, 1968)
- Butylon: o -Ethoxybenzamide3-Hydroxy- p -butyrophenetidide (Bucetin) (1966)
- Bucetin(3-hydroxy-p-butyrophenetidide)Phenacetin (1966)
- [Study on Butylon, a new combined analgesic, with special reference to the analgesic potentiation between o-ethoxybenzamide and 3-hydroxy-p-burtyrophenetidide (Bucetin)]. (Folia Pharmacologica Japonica, 1966)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - beta-hydroxybutyric acid-p-phenetidide
- NHB-PPT
- N-(beta-hydroxybutyryl)-p-phenetidine
-
SMILESCCOC1=CC=C(C=C1)NC(=O)CC(C)O
-
InChIKeyLIAWQASKBFCRNR-UHFFFAOYSA-N
- Pubchem - Bucetin
- Wikipedia - Bucetin
Bucetin (INN, BAN) is an analgesic and antipyretic that is no longer marketed. Chemically, it is similar to phenacetin with which it shares the risk of carcinogenesis. Bucetin was withdrawn from use in 1986 due to renal toxicity.
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Alternate Names
External Links
Synthesis
Reactant
+
4-ETHOXYANILINE
(Schotten-Baumann amide from acid)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
ETHYL HYDROPEROXIDE
(Dakin oxidation)
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(70-55-3)
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(7785-53-7, 98-55-5)
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(23981-47-7)
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Bucetin
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