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

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

tert-butyl 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate

tert-butyl 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate

((4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)methyl)triphenylphosphonium bromide

$300.00
CAS No.: 885477-83-8
Catalog No.: 109950
Purity: 95%
MF: C34H34BrFN3O2PS
MW: 678.608
Storage: 2-8 degree Celsius
SMILES: [Br-].CC(C)C1=C(C[P+](C2=CC=CC=C2)(C2=CC=CC=C2)C2=CC=CC=C2)C(=NC(=N1)N(C)S(C)(=O)=O)C1=CC=C(F)C=C1
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((4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)methyl)triphenylphosphonium bromide; CAS No.: 885477-83-8; As a worldwide chemical supplier, ChemShuttle provides phosphonium salts for ylide generation in olefination reactions. The triphenylphosphonium bromide moiety enables efficient Wittig reactions for statin side chain construction. Our quaternization process achieves >99% conversion through phase-transfer catalysis. The product s stability under anhydrous conditions ensures consistent performance in large-scale API synthesis.

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