6-(1-Hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-2-(2-methoxy-ethoxy)-nicotinonitrile

≥95%

Reagent Code: #196171
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CAS Number 1187187-28-5

science Other reagents with same CAS 1187187-28-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.11 g/mol
Formula C₁₆H₁₅BN₂O₅
thermostat Physical Properties
Boiling Point 508.0±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting BTK (Bruton's tyrosine kinase) for the treatment of autoimmune diseases and certain cancers. Its boron-containing structure enhances binding selectivity and potency in drug candidates. Also explored in prodrug formulations due to improved solubility and metabolic stability. Commonly applied in structure-activity relationship (SAR) studies to optimize pharmacokinetic properties in oncology and inflammation pipelines.

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inventory 5mg
10-20 days ฿26,130.00

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6-(1-Hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-2-(2-methoxy-ethoxy)-nicotinonitrile
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting BTK (Bruton's tyrosine kinase) for the treatment of autoimmune diseases and certain cancers. Its boron-containing structure enhances binding selectivity and potency in drug candidates. Also explored in prodrug formulations due to improved solubility and metabolic stability. Commonly applied in structure-activity relationship (SAR) studies to optimize pharmacokinetic properties in oncology a

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting BTK (Bruton's tyrosine kinase) for the treatment of autoimmune diseases and certain cancers. Its boron-containing structure enhances binding selectivity and potency in drug candidates. Also explored in prodrug formulations due to improved solubility and metabolic stability. Commonly applied in structure-activity relationship (SAR) studies to optimize pharmacokinetic properties in oncology and inflammation pipelines.

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