N-Boc-Pyrrolidin-2-(S)-ylboronic acid

97%

Reagent Code: #214763
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CAS Number 149716-79-0

science Other reagents with same CAS 149716-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.05 g/mol
Formula C₉H₁₈BNO₄
badge Registry Numbers
MDL Number MFCD17015042
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a chiral building block for the preparation of bioactive molecules, particularly in the development of pharmaceuticals. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds. The N-Boc protecting group enhances stability and solubility while enabling selective deprotection for further functionalization. The compound’s stereochemistry makes it valuable in asymmetric synthesis, especially in the construction of complex amines and heterocyclic compounds found in drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,840.00
500mg
10-20 days ฿19,920.00
N-Boc-Pyrrolidin-2-(S)-ylboronic acid
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Used in organic synthesis as a chiral building block for the preparation of bioactive molecules, particularly in the development of pharmaceuticals. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds. The N-Boc protecting group enhances stability and solubility while enabling selective deprotection for further functionalization. The compound’s stereochemistry makes it valuable in asymmetric synthesis, especial

Used in organic synthesis as a chiral building block for the preparation of bioactive molecules, particularly in the development of pharmaceuticals. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds. The N-Boc protecting group enhances stability and solubility while enabling selective deprotection for further functionalization. The compound’s stereochemistry makes it valuable in asymmetric synthesis, especially in the construction of complex amines and heterocyclic compounds found in drug candidates.

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