4-((5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methyl)morpholine

98%

Reagent Code: #241636
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CAS Number 919347-16-3

science Other reagents with same CAS 919347-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.19 g/mol
Formula C₁₆H₂₅BN₂O₃
badge Registry Numbers
MDL Number MFCD13191376
thermostat Physical Properties
Boiling Point 428.5±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its pyridine and morpholine moieties enhance solubility and binding properties, making it valuable in the development of kinase inhibitors and other bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting cancer, inflammation, and central nervous system disorders. The boronate ester group allows for efficient and selective coupling under mild conditions, ideal for late-stage functionalization in complex molecule assembly.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,760.00
inventory 250mg
10-20 days ฿27,510.00
4-((5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methyl)morpholine
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Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its pyridine and morpholine moieties enhance solubility and binding properties, making it valuable in the development of kinase inhibitors and other bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting cancer, inflammation, and central nervous system disorders. The boronate ester group allows for efficient and selecti

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its pyridine and morpholine moieties enhance solubility and binding properties, making it valuable in the development of kinase inhibitors and other bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting cancer, inflammation, and central nervous system disorders. The boronate ester group allows for efficient and selective coupling under mild conditions, ideal for late-stage functionalization in complex molecule assembly.

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