CAS 16064-08-7: 6-Iodo-4(3H)-quinazolinone
Formula:C8H5IN2O
InChI:InChI=1S/C8H5IN2O/c9-5-1-2-7-6(3-5)8(12)11-4-10-7/h1-4H,(H,10,11,12)
InChI key:InChIKey=PUGXMZKDRVGIHC-UHFFFAOYSA-N
SMILES:O=C1C=2C(=CC=C(I)C2)NC=N1
Synonyms:- 4(1H)-Quinazolinone, 6-iodo-
- 4(3H)-Quinazolinone, 6-iodo-
- 4-Quinazolinol, 6-iodo-
- 6-Iodo-1H-Quinazolin-4-One
- 6-Iodo-3,4-dihydroquinazolin-4-one
- 6-Iodo-3H-Quinazolin-4-One
- 6-Iodo-4(3H)-quinazolinone
- 6-Iodo-4-Quinazolone
- 6-Iodoquinazolin-4(1H)-One
- 6-Iodoquinazolin-4-One
- 6-Iodoquinazolinone
- See more synonyms
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Found 6 products.
6-Iodo-4-hydroxyquinazoline
CAS:Formula:C8H5IN2OPurity:>97.0%(GC)(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:272.056-IODOQUINAZOLIN-4-OL
CAS:Purity:95.0%Color and Shape:Solid, Slightly pale purple to pale purple powderMolecular weight:272.04501342773446-Iodoquinazolin-4-one
CAS:Controlled ProductApplications 6-Iodoquinazolin-4-one is an intermediate in the synthesis of Lapatinib (L175800). References Petrov, K., et al.: Bioorg. Med. Chem. Lett., 16, 4686 (2006),Formula:C8H5IN2OColor and Shape:NeatMolecular weight:272.056-IodoQuinazolin-4-ol
CAS:6-Iodoquinazolin-4-ol is a nitrogen nucleophile that reacts with formamide to produce chloroform, which has a strong odor. It can react with other nitrogen nucleophiles such as amines or ammonia to produce chloramines. 6-Iodoquinazolin-4-ol is not soluble in water, but is soluble in organic solvents such as ether. The compound is used in the synthesis of lapatinib and 2-chloro-5-iodobenzoic acid, which are cancer drugs. 6-Iodoquinazolin-4-ol is also used for the treatment of cancer cells and has been shown to inhibit the growth of human cancer cells by reacting with amines.Formula:C8H5IN2OPurity:Min. 95%Molecular weight:272.04 g/molRef: 3D-FI40532
Discontinued product
