tert-Butyl ((6-bromopyridin-3-yl)methyl)carbamate

97%

Reagent Code: #148221
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CAS Number 864266-29-5

science Other reagents with same CAS 864266-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.15 g/mol
Formula C₁₁H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD11052608
thermostat Physical Properties
Boiling Point 402.6±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling carbon–carbon bond formation. Also utilized in the preparation of pyridine-based derivatives for research in drug discovery and agrochemical development.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity 96.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿269.50
inventory 250mg
10-20 days ฿621.50
inventory 1g
10-20 days ฿2,960.00
inventory 5g
10-20 days ฿14,250.00

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tert-Butyl ((6-bromopyridin-3-yl)methyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling carbon–carbon bond formation. Also utilized in the preparation of pyridine-based derivatives for rese

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling carbon–carbon bond formation. Also utilized in the preparation of pyridine-based derivatives for research in drug discovery and agrochemical development.

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