(3R,5S,6E)-7-[4-(4-Fluorophenyl)-6-isopropyl-2-[(methanesulfonyl) methylamino]pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid tert-butyl ester

97%

Reagent Code: #230129
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CAS Number 355806-00-7

science Other reagents with same CAS 355806-00-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 537.64 g/mol
Formula C₂₆H₃₆FN₃O₆S
badge Registry Numbers
MDL Number MFCD08460212
thermostat Physical Properties
Boiling Point 704.1°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of certain 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 the protected hydroxy groups and functionalized pyrimidine core, it is valuable in multi-step organic transformations for producing potent lipid-regulating agents. Commonly employed in research and development settings for antihyperlipidemic drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿550.00
1g
10-20 days ฿1,260.00
5g
10-20 days ฿4,030.00
25g
10-20 days ฿13,630.00
(3R,5S,6E)-7-[4-(4-Fluorophenyl)-6-isopropyl-2-[(methanesulfonyl) methylamino]pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid tert-butyl ester
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Used as an intermediate in the synthesis of certain 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 the protected hydroxy groups and functionalized pyrimidine core, it is valuable in multi-step organic transformations for producing potent lipid-regulating agents. Commonly employed in research and development settings for antihyperlipidemic drug candidates.

Used as an intermediate in the synthesis of certain 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 the protected hydroxy groups and functionalized pyrimidine core, it is valuable in multi-step organic transformations for producing potent lipid-regulating agents. Commonly employed in research and development settings for antihyperlipidemic drug candidates.

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