1,2-Bis(bromomethyl)-4-(methylsulfonyl)benzene

95%

Reagent Code: #38815
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CAS Number 1802633-31-3

science Other reagents with same CAS 1802633-31-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.05 g/mol
Formula C₉H₁₀Br₂O₂S
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily as a key intermediate in organic synthesis, this compound is valuable in the production of pharmaceuticals and agrochemicals. Its reactive bromomethyl groups enable it to participate in various coupling and substitution reactions, making it useful for constructing complex molecular structures. Additionally, it serves as a precursor in the development of sulfonamide-based compounds, which are widely used in medicinal chemistry for their antibacterial and anti-inflammatory properties. Its methylsulfonyl group further enhances its utility in creating molecules with specific biological activities.

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inventory 100mg
10-20 days ฿33,930.00

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1,2-Bis(bromomethyl)-4-(methylsulfonyl)benzene
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Used primarily as a key intermediate in organic synthesis, this compound is valuable in the production of pharmaceuticals and agrochemicals. Its reactive bromomethyl groups enable it to participate in various coupling and substitution reactions, making it useful for constructing complex molecular structures. Additionally, it serves as a precursor in the development of sulfonamide-based compounds, which are widely used in medicinal chemistry for their antibacterial and anti-inflammatory properties. Its me

Used primarily as a key intermediate in organic synthesis, this compound is valuable in the production of pharmaceuticals and agrochemicals. Its reactive bromomethyl groups enable it to participate in various coupling and substitution reactions, making it useful for constructing complex molecular structures. Additionally, it serves as a precursor in the development of sulfonamide-based compounds, which are widely used in medicinal chemistry for their antibacterial and anti-inflammatory properties. Its methylsulfonyl group further enhances its utility in creating molecules with specific biological activities.

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