6-Chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

98%

Reagent Code: #192941
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CAS Number 1073353-82-8

science Other reagents with same CAS 1073353-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.58 g/mol
Formula C₁₅H₁₉BClNO₂
badge Registry Numbers
MDL Number MFCD11504964
thermostat Physical Properties
Boiling Point 419.6±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex indole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development of bioactive molecules. Commonly applied in the preparation of drug candidates targeting neurological disorders, inflammation, and cancer due to the indole scaffold’s prevalence in medicinal chemistry. Stable and compatible with a wide range of functional groups, it supports late-stage functionalization in organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,120.00
inventory 500mg
10-20 days ฿6,600.00
inventory 1g
10-20 days ฿11,000.00

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6-Chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex indole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development of bioactive molecules. Commonly applied in the preparation of drug candidates targeting neurological disorders, inflammation, and cancer due to the indole scaffold’s prevalence in medicinal chemistry. Stable and compatible with a wide range of functional groups, it supports late-stage functionalization in organic synthesis.
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