tert-Butyl 5-bromo-2-methyl-1H-benzo[d]imidazole-1-carboxylate

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Reagent Code: #192454
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CAS Number 1038392-63-0

science Other reagents with same CAS 1038392-63-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.17 g/mol
Formula C₁₃H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD30067358
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization at the bromo position, enabling coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic or heteroaromatic groups. The tert-butoxycarbonyl (Boc) protecting group stabilizes the imidazole nitrogen during multi-step syntheses and can be easily removed under mild acidic conditions when needed. Commonly employed in medicinal chemistry for constructing bioactive molecules targeting inflammation, cancer, and central nervous system disorders.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿6,990.00
1g
10-20 days ฿19,020.00
100mg
10-20 days ฿3,960.00
tert-Butyl 5-bromo-2-methyl-1H-benzo[d]imidazole-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization at the bromo position, enabling coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic or heteroaromatic groups. The tert-butoxycarbonyl (Boc) protecting group stabilizes the imidazole nitrogen during multi-step syntheses and can be easily removed under mild acidic conditions when needed. Commonly employed in medicinal chemistry for constructing bioactive molecules targeting inflammation, cancer, and central nervous system disorders.
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