2-(aminomethyl)-4-tert-butyl-6-iodophenol
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2-(aminomethyl)-4-tert-butyl-6-iodophenol
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CAS No:
58456-91-0
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Formula:
C11H16INO
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Chemical Name:
2-(aminomethyl)-4-tert-butyl-6-iodophenol
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Synonyms:
2-aminomethyl-4-butyl-6-iodophenyl;2-aminomethyl-4-t-butyl-6-iodophenol;2-aminomethyl-4-t-butyl-6-iodophenol hydrochloride;MK 447;MK-447;58456-91-0;MK-447;2-Aminomethyl-4-t-butyl-6-iodophenol;2-(aminomethyl)-4-tert-butyl-6-iodophenol;Phenol, 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodo-;MK 447;SCHEMBL888409;2-(Aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol;CHEMBL279581;DTXSID00207153;ZINC1869856;DA-27917;HY-100297;CS-0018449;FT-0737268;2-AMINOMETHYL-4-TERT-BUTYL-6-IODOPHENOL;2-aminomethyl-4-(1,1-dimethylethyl)-6-iodophenol
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CAS No:
2-(aminomethyl)-4-tert-butyl-6-iodophenol Basic Attributes
305.15 g/mol
305.02766 g/mol
DTXSID00207153
Drug Information
Agents that promote the excretion of urine through their effects on kidney function. (See all compounds classified as Diuretics.)|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.)
2-aminomethyl-4-butyl-6-iodophenyl
Computed Properties
Molecular Weight:305.15
XLogP3:3.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:305.02766
Monoisotopic Mass:305.02766
Topological Polar Surface Area:46.2
Heavy Atom Count:14
Complexity:190
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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