3-Bromo-N-(tert-butyl)benzenesulfonamide

98%

Reagent Code: #50862
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CAS Number 308283-47-8

science Other reagents with same CAS 308283-47-8

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Weight 292.1900 g/mol
Formula C₁₀H₁₄BrNO₂S
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MDL Number MFCD07363824
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the development of pharmaceutical compounds, particularly in the creation of sulfonamide-based drugs, which are known for their antibacterial and diuretic properties. Additionally, it serves as a key building block in the synthesis of complex molecules for research purposes, aiding in the study of new chemical reactions and pathways. Its tert-butyl group provides steric hindrance, making it useful in selective reactions and protecting group strategies in synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿810.00
inventory 5g
10-20 days ฿5,930.00
inventory 25g
10-20 days ฿25,750.00
inventory 1g
10-20 days ฿1,560.00

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3-Bromo-N-(tert-butyl)benzenesulfonamide
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the development of pharmaceutical compounds, particularly in the creation of sulfonamide-based drugs, which are known for their antibacterial and diuretic properties. Additionally, it serves as a key building block in the synthesis of complex molecules for research purposes, aiding in the study of new chemical reactions and pathways. Its tert-butyl group provides steric hindrance, making it usefu

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the development of pharmaceutical compounds, particularly in the creation of sulfonamide-based drugs, which are known for their antibacterial and diuretic properties. Additionally, it serves as a key building block in the synthesis of complex molecules for research purposes, aiding in the study of new chemical reactions and pathways. Its tert-butyl group provides steric hindrance, making it useful in selective reactions and protecting group strategies in synthetic chemistry.

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