4-Bromo-N-tert-butyl-3-methylbenzenesulfonamide

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Reagent Code: #215501
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CAS Number 958651-46-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.22 g/mol
Formula C₁₁H₁₆BrNO₂S
badge Registry Numbers
MDL Number MFCD12650344
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its sulfonamide group and bromo substituent make it valuable for cross-coupling reactions, enabling the construction of complex aromatic systems. Commonly employed in the preparation of bioactive molecules, including potential kinase inhibitors and anti-inflammatory agents. The tert-butyl group enhances lipophilicity and steric bulk, which can influence metabolic stability and binding selectivity in drug design. Also utilized in research settings for the synthesis of sulfonamide-based libraries for high-throughput screening.

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inventory 5g
10-20 days ฿21,600.00

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4-Bromo-N-tert-butyl-3-methylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its sulfonamide group and bromo substituent make it valuable for cross-coupling reactions, enabling the construction of complex aromatic systems. Commonly employed in the preparation of bioactive molecules, including potential kinase inhibitors and anti-inflammatory agents. The tert-butyl group enhances lipophilicity and steric bulk, which can influence metabolic stability and binding selec

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its sulfonamide group and bromo substituent make it valuable for cross-coupling reactions, enabling the construction of complex aromatic systems. Commonly employed in the preparation of bioactive molecules, including potential kinase inhibitors and anti-inflammatory agents. The tert-butyl group enhances lipophilicity and steric bulk, which can influence metabolic stability and binding selectivity in drug design. Also utilized in research settings for the synthesis of sulfonamide-based libraries for high-throughput screening.

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