O-Fluoroaniline isomer of Ezetimibe

Product Name O-Fluoroaniline isomer of Ezetimibe
Alternate Names Ezetimibe Impurities, Impurities of Ezetimibe
CAT No. CS-O-14869
CAS No. Not Available
Category Impurities
Stock IN-Stock
Mol. Wt. 409.43 g/mol
Mol. For. C₂₄H₂₁F₂NO₃
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Ezetimibe
Purity >98%
Therapeutic Anti-Hyperlipidemics
Smileys O[C@@H](CC[C@@H]1[C@H](N(C1=O)C2=C(C=CC=C2)F)C3=CC=C(C=C3)O)C4=CC=C(C=C4)F
Controlled No
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O-Fluoroaniline is a chemical compound that is used as an intermediate in the synthesis of various drugs such as Ezetimibe. Ezetimibe is a medication used to lower cholesterol levels in the blood, which is a major risk factor for heart disease. The O-Fluoroaniline isomer of Ezetimibe is a key intermediate in the synthesis of this medication. The chemical structure of O-Fluoroaniline isomer of Ezetimibe consists of a fluorine atom attached to an aniline group. It is a white to off-white solid with a melting point of around 62-64°C. O-Fluoroaniline isomer of Ezetimibe is soluble in organic solvents such as methanol, ethanol, and acetone. In the synthesis of Ezetimibe, O-Fluoroaniline isomer of Ezetimibe is reacted with various other chemicals to form the final product. The chemical reaction involves the formation of a carbon-nitrogen bond between the aniline group of O-Fluoroaniline isomer of Ezetimibe and another chemical called phthalic anhydride. This reaction is known as the Friedel-Crafts acylation reaction. In conclusion, O-Fluoroaniline isomer of Ezetimibe is an important intermediate in the synthesis of Ezetimibe, a medication used to lower cholesterol levels in the blood. Its chemical structure and properties make it a suitable reagent for the Friedel-Crafts acylation reaction, which is used in the synthesis of various pharmaceuticals.

Related Compounds

SSR-Ezetimibe | Ezetimibe Impurity B | Ezetimibe tetrahydropyran analog | Ezetimibe impurity (3-[5-(4-Fluoro-phenyl)-5-(R)-hydroxy-pentanoyl]-4-(S)-phenyl-oxazolidin-2-one) | Ezetimibe Diol Impurity | Ezetimibe Impurity 10 | Ezetimibe Lactone Impurity | Ezetimibe 2-Fluoro impurity | Ezetimibe Impurity 18 | ent-Ezetimibe | Benzyl Ezetimibe ether | Ezetimibe Impurity C | Ezetimibe Ring-opening Dehydrate Impurity | O-Fluorobenzene isomer of Ezetimibe | Ezetimibe Impurity 25 | Ezetimibe Didesfluro impurity | Ezetimibe Diacid | Ezetimibe O-trimethylsilyl O-benzyl Impurity | Benzylated Ezetimibe | Ezetimibe (3R,4R,3'R)-Isomer | Ezetimibe 2-Fluoro Hydroxy impurity | Ezetimibe Impurity 11 | Ezetimibe Triol Impurity | Methyl 5-(4-Fluorophenyl)-(5S)-hydroxypentanoate | Ezetimibe Azetidinone Ring opened impurity | m-Fluoroaniline isomer of Ezetimibe | Ezetimibe Impurity 1 ((3'S,3R,4S)-Desfluoro Ezetimibe) | Ezetimibe Related Impurity 7 | RSR Ezetimibe | Ezetimibe ring open impurity | Ezetimibe Deprotected Impurity | RRR-Ezetimibe+SSS-Ezetimibe (Diastereomer mixture) | Ezetimibe Benzyl Impurity (MBZT-2) | Ezetimibe Benzyl Diol Impurity | Ezetimibe Dides fluoro impurity | Ezetimibe Impurity 17 | Ezetimibe (3S,4S,3'R)-Isomer | Ezetimibe Desfluoro impurity | Ezetimibe Lactam Cleaved Alcohol | Ezetimibe Trihydroxy Impurity | Ezetimibe Impurity 15 | N-Nitroso Ezetimibe Impurity |

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