Methyl()-(3-R)-7-[4-(4-Fluorophenyl)-6-isopropyl-2-(N-methyl-N-methanesul fonylamino) pyrimidin-5-yl]-3-hydroxy-5-oxo-6(E)-heptenoate

97%

Reagent Code: #208180
fingerprint
CAS Number 147118-39-6

science Other reagents with same CAS 147118-39-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 493.5483 g/mol
Formula C₂₃H₂₈FN₃O₆S
badge Registry Numbers
MDL Number MFCD12755726
thermostat Physical Properties
Boiling Point 701.7℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.311g/ml
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of statin-class cholesterol-lowering drugs. Its structure supports the formation of active pharmaceutical ingredients that inhibit HMG-CoA reductase, a key enzyme in cholesterol biosynthesis. Due to its functional groups—such as the hydroxyl, keto, and ester moieties—it participates in selective reductions and coupling reactions during drug manufacturing. Commonly employed in controlled environments to produce high-purity metabolites and analogs for cardiovascular therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,690.00
Methyl()-(3-R)-7-[4-(4-Fluorophenyl)-6-isopropyl-2-(N-methyl-N-methanesul fonylamino) pyrimidin-5-yl]-3-hydroxy-5-oxo-6(E)-heptenoate
No image available

Used primarily as an intermediate in the synthesis of statin-class cholesterol-lowering drugs. Its structure supports the formation of active pharmaceutical ingredients that inhibit HMG-CoA reductase, a key enzyme in cholesterol biosynthesis. Due to its functional groups—such as the hydroxyl, keto, and ester moieties—it participates in selective reductions and coupling reactions during drug manufacturing. Commonly employed in controlled environments to produce high-purity metabolites and analogs for card

Used primarily as an intermediate in the synthesis of statin-class cholesterol-lowering drugs. Its structure supports the formation of active pharmaceutical ingredients that inhibit HMG-CoA reductase, a key enzyme in cholesterol biosynthesis. Due to its functional groups—such as the hydroxyl, keto, and ester moieties—it participates in selective reductions and coupling reactions during drug manufacturing. Commonly employed in controlled environments to produce high-purity metabolites and analogs for cardiovascular therapeutics.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...