Epirizole
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Epirizole
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CAS No:
18694-40-1
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Formula:
C11H14N4O2
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Chemical Name:
Epirizole
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Synonyms:
Pyrimidine,4-methoxy-2-(5-methoxy-3-methyl-1H-pyrazol-1-yl)-6-methyl-;Pyrimidine,4-methoxy-2-(5-methoxy-3-methylpyrazol-1-yl)-6-methyl-;4-Methoxy-2-(5-methoxy-3-methyl-1H-pyrazol-1-yl)-6-methylpyrimidine;1-(4-Methyl-6-methoxy-2-pyrimidinyl)-3-methyl-5-methoxypyrazole;DA 398;Mepirizole;1-(4-Methoxy-6-methyl-2-pyrimidinyl)-3-methyl-5-methoxypyrazole;4-Methoxy-2-(5-methoxy-3-methylpyrazol-1-yl)-6-methylpyrimidine;2-(3-Methyl-5-methoxy-1-pyrazolyl)-4-methoxy-6-methylpyrimidine;2-(3-Methoxy-5-methylpyrazol-2-yl)-4-methoxy-6-methylpyrimidine;Mebron;Epirizole
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CAS No:
Description
Epirizole is an aromatic ether.|Epirizole is an oral nonsteroidal anti-inflammatory drug (NSAID) used for muscle and joint pain.|4-Methoxy-2-(5-methoxy-3-methylpyrazol-1-yl)-6-methylpyrimidine. A pyrimidinyl pyrazole with antipyretic, analgesic, and anti-inflammatory activity.
Characteristics
62.1
1.29630
Yellow power
1.1972 (rough estimate)
90-92 °C
376.57°C (rough estimate)
222.3ºC
1.6000 (estimate)
>35.1 [ug/mL]
2-8°C
0mmHg at 25°C
LD50 orally in mice: 820 mg/kg (Ogura)
Safety Information
NONH for all modes of transport
3
20/21/22-36/37/38
26-36
UV9290000
Xn
Stable at normal temperatures and pressures.
P261-P280-P305 + P351 + P338
H302-H312-H315-H319-H332-H335
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)
Epirizole
Computed Properties
Molecular Weight:234.25
XLogP3:1.3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:234.11167570
Monoisotopic Mass:234.11167570
Topological Polar Surface Area:62.1
Heavy Atom Count:17
Complexity:254
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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