(R)-tert-butyl (1-([1,1'-biphenyl]-4-yl)-3-hydroxypropan-2-yl)carbaMate

98%

Reagent Code: #202225
label
Alias LCZ696 intermediate
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CAS Number 1426129-50-1

science Other reagents with same CAS 1426129-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.42 g/mol
Formula C₂₀H₂₅NO₃
thermostat Physical Properties
Melting Point 114 - 116 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical agents, particularly in the development of beta-blockers and other cardiovascular drugs. Its chiral structure makes it valuable in enantioselective synthesis, where the (R)-enantiomer contributes to higher biological activity and selectivity. Commonly employed in the preparation of protease inhibitors and antihypertensive compounds due to its ability to enhance metabolic stability and binding affinity. Also utilized in research settings for asymmetric synthesis and development of novel chiral building blocks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿580.00
inventory 25g
10-20 days ฿2,110.00
inventory 100g
10-20 days ฿8,150.00
inventory 500g
10-20 days ฿39,130.00
(R)-tert-butyl (1-([1,1'-biphenyl]-4-yl)-3-hydroxypropan-2-yl)carbaMate
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Used as an intermediate in the synthesis of pharmaceutical agents, particularly in the development of beta-blockers and other cardiovascular drugs. Its chiral structure makes it valuable in enantioselective synthesis, where the (R)-enantiomer contributes to higher biological activity and selectivity. Commonly employed in the preparation of protease inhibitors and antihypertensive compounds due to its ability to enhance metabolic stability and binding affinity. Also utilized in research settings for asymm

Used as an intermediate in the synthesis of pharmaceutical agents, particularly in the development of beta-blockers and other cardiovascular drugs. Its chiral structure makes it valuable in enantioselective synthesis, where the (R)-enantiomer contributes to higher biological activity and selectivity. Commonly employed in the preparation of protease inhibitors and antihypertensive compounds due to its ability to enhance metabolic stability and binding affinity. Also utilized in research settings for asymmetric synthesis and development of novel chiral building blocks.

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