7-Bromooxazolo[4,5-c]pyridine

≥95%

Reagent Code: #148428
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CAS Number 1256822-23-7

science Other reagents with same CAS 1256822-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.01 g/mol
Formula C₆H₃BrN₂O
badge Registry Numbers
MDL Number MFCD08692341
thermostat Physical Properties
Boiling Point 268.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly kinase inhibitors and other bioactive molecules targeting central nervous system disorders. Its structure enables selective functionalization, making it valuable in medicinal chemistry for developing novel drug candidates. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in the preparation of receptor modulators and enzyme inhibitors due to its favorable electronic and steric properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,880.00
inventory 250mg
10-20 days ฿19,050.00
inventory 1g
10-20 days ฿47,640.00

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7-Bromooxazolo[4,5-c]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly kinase inhibitors and other bioactive molecules targeting central nervous system disorders. Its structure enables selective functionalization, making it valuable in medicinal chemistry for developing novel drug candidates. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in the preparation of receptor modulators and

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly kinase inhibitors and other bioactive molecules targeting central nervous system disorders. Its structure enables selective functionalization, making it valuable in medicinal chemistry for developing novel drug candidates. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in the preparation of receptor modulators and enzyme inhibitors due to its favorable electronic and steric properties.

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