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ChemicalBook--->CAS DataBase List--->417717-21-6

417717-21-6

417717-21-6 Structure

417717-21-6 Structure
IdentificationBack Directory
[Name]

Lenvatinib Impurity f
[CAS]

417717-21-6
[Synonyms]

Lenvatinib Impurity f
Levatinib Impurity 11
Lenvatinib Carboxylic Acid
4-(3-chloro-4-(3-cyclopropylureido)phenoxy)-7-methoxyquinoline-6-carboxylic acid
4-[3-Chloro-4-[[(cyclopropylamino)carbonyl]amino]phenoxy]-7-methoxy-6-quinolinecarboxylic acid
6-Quinolinecarboxylic acid, 4-[3-chloro-4-[[(cyclopropylamino)carbonyl]amino]phenoxy]-7-methoxy-
[Molecular Formula]

C21H18ClN3O5
[MDL Number]

MFCD32182568
[MOL File]

417717-21-6.mol
[Molecular Weight]

427.84
Chemical PropertiesBack Directory
[Boiling point ]

599.5±50.0 °C(Predicted)
[density ]

1.50±0.1 g/cm3(Predicted)
[pka]

2.74±0.30(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Desamino Hydroxy Lenvatinib serves as a reagent for the synthesis of urea derivatives containing nitrogenous aromatic ring compounds that functions as angiogenesis inhibitors for treatment of diseases. It is also a derivative compound of Lenvatinib (L329400) that serves as orally active inhibitor of multiple receptor tyrosine kinases including VEGF, FGF and SCF receptors.
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