ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-4-fluoro-1H-indazol-3-yl)-2-oxocyclohex-3-ene-1-carboxylate

ethyl 4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-4-fluoro-1H-indazol-3-yl)-2-oxocyclohex-3-ene-1-carboxylate

N-cyclohexyl-3-((2,3-dihydrobenzo[b][1,4]dioxine)-6-sulfonamido)-4-(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)benzamide

N-cyclohexyl-3-((2,3-dihydrobenzo[b][1,4]dioxine)-6-sulfonamido)-4-(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)benzamide

(1S,2S)-4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-4-fluoro-1H-indazol-3-yl)-2-hydroxycyclohex-3-ene-1-carboxylic acid

$408.00
CAS No.: 1562374-72-4
Catalog No.: 198454
Purity: 95%
MF: C22H15ClF4N2O4
MW: 482.817
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C(=O)N2N=C(C3=C(C=CC=C23)F)C2=C[C@@H]([C@H](CC2)C(=O)O)O)C(=CC=C1)C(F)(F)F
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CAS No.:1562374-72-4;(1S,2S)-4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-4-fluoro-1H-indazol-3-yl)-2-hydroxycyclohex-3-ene-1-carboxylic acid;As a premier chemical synthesis company specializing in complex heterocyclic compounds, ChemShuttle offers the (1S,2S)-4-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-4-fluoro-1H-indazol-3-yl)-2-hydroxycyclohex-3-ene-1-carboxylic acid (CAS No.:1562374-72-4). This compound represents the cutting edge of our chemical building blocks designed for advanced drug discovery and development. The molecule integrates multiple pharmacophores: a chiral cyclohexene core with a hydroxyl group, an indazole ring substituted with a fluoro group, and a benzoyl moiety carrying a chloro and trifluoromethyl group. Such a combination creates a versatile platform for further functionalization and target engagement. As a worldwide chemical supplier, we ensure the availability of such specialized intermediates, supporting researchers in their quest for novel therapeutic agents. Our custom synthesis services can modify this compound to incorporate additional functionalities or modify existing ones, enhancing its utility as a key intermediate in drug development. The strategic placement of the hydroxyl, carboxylic acid, and multiple aromatic substituents provides numerous points for chemical modification. This allows for the creation of diverse libraries of compounds for biological screening, making it an invaluable asset in the pursuit of innovative therapeutic solutions.

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