1H-Indole-1-carboxylic acid, 4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester

≥95%

Reagent Code: #191946
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CAS Number 1256359-94-0

science Other reagents with same CAS 1256359-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 377.6701 g/mol
Formula C₁₉H₂₅BClNO₄
badge Registry Numbers
MDL Number MFCD16036140
thermostat Physical Properties
Boiling Point 479.5±48.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage -20°C

description Product Description

Used primarily as an intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly applied in the preparation of indole-based drug candidates, including those targeting inflammation, cancer, and neurological disorders. The tert-butyl ester group offers stability during reactions and can be easily deprotected when needed. Preferred in research settings for its reliability in generating complex molecular structures with high yields.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,420.00
inventory 250mg
10-20 days ฿20,800.00

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1H-Indole-1-carboxylic acid, 4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
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Used primarily as an intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly applied in the preparation of indole-based drug candidates, including those targeting inflammation, cancer, and neurological disorders. The tert-butyl ester group offers stability during reactions and can be easily deprotected when needed. Preferred in research settings for its reliability in generating complex molecular structures with high yields.
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