(4R,6S)-6-[(1E)-2-[2-cyclopropyl-4-(4-fluorophenyl)-3-quinolinyl]ethenyl]-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester

(4R,6S)-6-[(1E)-2-[2-cyclopropyl-4-(4-fluorophenyl)-3-quinolinyl]ethenyl]-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester

N-[4-[(7-chloro-2,3,4,5-tetrahydro-5-oxo-1H-1-benzazepin-1-yl)carbonyl]-3-methylphenyl]-2-methylbenzamide

N-[4-[(7-chloro-2,3,4,5-tetrahydro-5-oxo-1H-1-benzazepin-1-yl)carbonyl]-3-methylphenyl]-2-methylbenzamide

tert-butyl (4R,6R)-2-[[[6-(2-4-fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)pyrrol-1-yl]ethyl]-2,2-dimethyl-1,3-dioxan-4-yl]acetate

$250.00
CAS No.: 125971-95-1
Catalog No.: 109978
Purity: 95%
MF: C40H47FN2O5
MW: 654.823
Storage: 2-8 degree Celsius
SMILES: CC(C)C1=C(C(=O)NC2=CC=CC=C2)C(=C(N1CC[C@@H]1C[C@H](CC(=O)OC(C)(C)C)OC(C)(C)O1)C1=CC=C(F)C=C1)C1=CC=CC=C1
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tert-butyl (4R,6R)-2-[[[6-(2-4-fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)pyrrol-1-yl]ethyl]-2,2-dimethyl-1,3-dioxan-4-yl]acetate; CAS No.: 125971-95-1; ChemShuttle s building blocks for drug discovery include this fluorophenyl-pyrrole-dioxane hybrid, designed as a PPAR modulator. The carbamoyl group and multiple aryl substituents enable nuclear receptor subtype selectivity. Our Paal-Knorr synthesis optimizes pyrrole ring formation with electron-deficient amines. The product supports development of dual PPAR / agonists for metabolic syndrome treatment.

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