![5-(bromomethyl)-4-(4-fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/0/109948_2.jpg)
![methyl 4-(4-fluorophenyl)-6-isopropyl-2-[(N-methyl-N-methylsulfonyl)amino]pyrimidine-5-carboxylate](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/0/109946_2.jpg)
4-(4-fluorophenyl)-6-isopropyl-2-[(N-methyl-n-methylsulfonyl)amino]pyrimidine-5-yl-methanol
$200.00
CAS No.: 147118-36-3
Catalog No.: 109947
Purity: 95%
MF: C16H20FN3O3S
MW: 353.419
Storage: 2-8 degree Celsius
SMILES: CC(C)C1=C(CO)C(=NC(=N1)N(C)S(C)(=O)=O)C1=CC=C(F)C=C1
Catalog No.: 109947
Purity: 95%
MF: C16H20FN3O3S
MW: 353.419
Storage: 2-8 degree Celsius
SMILES: CC(C)C1=C(CO)C(=NC(=N1)N(C)S(C)(=O)=O)C1=CC=C(F)C=C1
4-(4-fluorophenyl)-6-isopropyl-2-[(N-methyl-n-methylsulfonyl)amino]pyrimidine-5-yl-methanol; CAS No.: 147118-36-3; This pyrimidine methanol derivative represents ChemShuttle s key intermediates for side chain elongation in statin synthesis. The benzylic alcohol undergoes smooth oxidation to aldehyde for subsequent Wittig reactions. Our borohydride reduction protocols achieve complete conversion without over-reduction byproducts. The product s stability under acidic conditions enables its use in multi-step synthetic sequences.
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