(S)-tert-Butyl (3-hydroxy-1, 1-diphenylpropan-2-yl)carbamate

98%

Reagent Code: #236527
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CAS Number 155836-47-8

science Other reagents with same CAS 155836-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.42 g/mol
Formula C₂₀H₂₅NO₃
badge Registry Numbers
MDL Number MFCD01863566
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of β-adrenergic receptor blockers and other bioactive molecules. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, making it valuable in asymmetric synthesis. The compound's stereochemistry supports high enantioselectivity in drug synthesis, improving efficacy and reducing side effects in final active pharmaceutical ingredients. Commonly employed in research settings for building complex organic molecules with defined spatial orientation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,320.00
inventory 250mg
10-20 days ฿3,110.00
(S)-tert-Butyl (3-hydroxy-1, 1-diphenylpropan-2-yl)carbamate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of β-adrenergic receptor blockers and other bioactive molecules. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, making it valuable in asymmetric synthesis. The compound's stereochemistry supports high enantioselectivity in drug synthesis, improving efficacy and reducing side effects in final active pharmaceutical ingredients. Commonly employed in research settings f

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of β-adrenergic receptor blockers and other bioactive molecules. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, making it valuable in asymmetric synthesis. The compound's stereochemistry supports high enantioselectivity in drug synthesis, improving efficacy and reducing side effects in final active pharmaceutical ingredients. Commonly employed in research settings for building complex organic molecules with defined spatial orientation.

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