CAS 885950-46-9
:Formula:C7H6INO3
InChI:InChI=1S/C7H6INO3/c1-12-7(11)4-2-5(8)6(10)9-3-4/h2-3H,1H3,(H,9,10)
InChI key:LHGAGXUKDZFFSF-UHFFFAOYSA-N
SMILES:COC(=O)C1=CNC(=O)C(=C1)I
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Methyl 1,6-dihydro-5-iodo-6-oxopyridine-3-carboxylate
CAS:Methyl 1,6-dihydro-5-iodo-6-oxopyridine-3-carboxylateFormula:C7H6INO3Purity:≥95%Color and Shape:SolidMolecular weight:279.03191Methyl 6-hydroxy-5-iodonicotinate
CAS:Methyl 6-hydroxy-5-iodonicotinateFormula:C7H6INO3Purity:≥95%Color and Shape:SolidMolecular weight:279.03191Methyl 6-hydroxy-5-iodonicotinate
CAS:Formula:C7H6INO3Purity:95%Color and Shape:SolidMolecular weight:279.0319METHYL 6-HYDROXY-5-IODONICOTINATE
CAS:Formula:C7H6INO3Purity:95%Color and Shape:SolidMolecular weight:279.033Methyl 6-hydroxy-5-iodonicotinate
CAS:Methyl 6-hydroxy-5-iodonicotinateFormula:C7H6INO3Purity:98%Molecular weight:279.03Methyl 6-hydroxy-5-iodonicotinate
CAS:Methyl 6-hydroxy-5-iodonicotinate (6HI) is an industrialization product that can be synthesized by the chlorination of methyl 5-hydroxy-2-iodonicotinate (5HI), followed by a reduction reaction. The target compound can then be obtained in high yield and purity through the facilitation of tert-butyl chloride. A number of synthesis methods have been developed for this process, including a nucleophilic substitution reaction with an alkynyl or alkyne as the electrophile, and a cyclization reaction. The synthesis method is repeatable and high yielding, making it suitable for commercial use.Formula:C7H6INO3Purity:Min. 95%Molecular weight:279 g/molRef: 3D-KKB95046
Discontinued product
