2-Cyclopropyl-4-(4-fluorophenyl)-3-quinoline-d5 3-Aldehyde

Product Name 2-Cyclopropyl-4-(4-fluorophenyl)-3-quinoline-d5 3-Aldehyde
CAT No. CS-T-73881
CAS No. 1346597-84-9
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys C1CC1C2=NC3=CC=CC=C3C(=C2C=O)C4=CC=C(C=C4)F
Canonical Smiles C1CC1C2=NC3=CC=CC=C3C(=C2C=O)C4=CC=C(C=C4)F
InchIKey JAHBIRPTCXOGLB-ZUIAZTCQSA-N
Inchl InChI=1S/C19H14FNO/c20-14-9-7-12(8-10-14)18-15-3-1-2-4-17(15)21-19(13-5-6-13)16(18)11-22/h1-4,7-11,13H,5-6H2/i5D2,6D2,13D
IUPAC 4-(4-fluorophenyl)-2-(1,2,2,3,3-pentadeuteriocyclopropyl)quinoline-3-carbaldehyde
Controlled No
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2-Cyclopropyl-4-(4-fluorophenyl)-3-quinoline-d5 3-Aldehyde is a deuterated analog of a quinoline compound with potential antineoplastic activity. This compound is usually used in the synthesis of drug candidates for cancer treatment. The chemical formula for 2-Cyclopropyl-4-(4-fluorophenyl)-3-quinoline-d5 3-Aldehyde is C19H10D5FNO and it has a molecular weight of 298.37 g/mol. Its melting point is 181-183°C and its boiling point is 514.2°C. The compound is soluble in organic solvents such as chloroform and dichloromethane. This compound has a unique chemical structure that makes it a promising candidate for cancer treatment. It is a quinoline derivative, which is a class of compounds known for their potential as anticancer agents. The presence of a cyclopropyl group in the structure of 2-Cyclopropyl-4-(4-fluorophenyl)-3-quinoline-d5 3-Aldehyde enhances its activity as a cancer drug by increasing its potency and selectivity towards cancer cells. In conclusion, 2-Cyclopropyl-4-(4-fluorophenyl)-3-quinoline-d5 3-Aldehyde is a deuterated analog of a quinoline compound with potential antineoplastic activity that is usually used in the synthesis of drug candidates for cancer treatment. Its unique chemical structure and solubility properties make it a promising candidate for further research in the field of cancer drug development.

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