((3S,5R)-5-((1H-1,2,4-triazol-1-yl)methyl)-5-(2,4-difluorophenyl)-tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate

((3S,5R)-5-((1H-1,2,4-triazol-1-yl)methyl)-5-(2,4-difluorophenyl)-tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate

N-[5-(diphenylphosphinoylmethyl)-4-(4-fluorophenyl)-6-isopropylpyrimidin-2-yl]-N-methylmethanesulfonamide

N-[5-(diphenylphosphinoylmethyl)-4-(4-fluorophenyl)-6-isopropylpyrimidin-2-yl]-N-methylmethanesulfonamide

2-[(1S,2S)-1-ethyl-2-bezyloxypropyl]-2,4-dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3-one

$250.00
CAS No.: 184177-83-1
Catalog No.: 109939
Purity: 95%
MF: C30H35N5O3
MW: 513.642
Storage: 2-8 degree Celsius
SMILES: CC[C@@H]([C@H](C)OCC1=CC=CC=C1)N1N=CN(C1=O)C1=CC=C(C=C1)N1CCN(CC1)C1=CC=C(O)C=C1
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2-[(1S,2S)-1-ethyl-2-bezyloxypropyl]-2,4-dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3-one; CAS No.: 184177-83-1; This triazolone derivative highlights ChemShuttle s heterocycles portfolio for antifungal research. The 4-hydroxyphenyl-piperazinyl group enables CYP51 enzyme targeting, while the bezyloxypropyl chain optimizes membrane permeability. Our regioselective triazolone formation prevents dimerization side products. The product serves as a lead compound for azole-resistant candidiasis treatment development.

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