1-(Bromomethyl)-3-isopropylbenzene

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Reagent Code: #129184
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CAS Number 75369-42-5

science Other reagents with same CAS 75369-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.118 g/mol
Formula C₁₀H₁₃Br
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its reactive bromomethyl group allows for easy alkylation and attachment to other molecular frameworks. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the isopropylbenzene moiety is part of the target structure. Also utilized in the synthesis of functionalized polymers and specialty chemicals due to its ability to undergo substitution reactions with nucleophiles. Its stability and reactivity profile make it suitable for controlled reactions in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿57,790.00

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1-(Bromomethyl)-3-isopropylbenzene
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Used as a key intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its reactive bromomethyl group allows for easy alkylation and attachment to other molecular frameworks. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the isopropylbenzene moiety is part of the target structure. Also utilized in the synthesis of functionalized polymers and specialty chemicals due to its ability to undergo substitution reactions with nucleophiles. Its

Used as a key intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its reactive bromomethyl group allows for easy alkylation and attachment to other molecular frameworks. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the isopropylbenzene moiety is part of the target structure. Also utilized in the synthesis of functionalized polymers and specialty chemicals due to its ability to undergo substitution reactions with nucleophiles. Its stability and reactivity profile make it suitable for controlled reactions in multi-step synthetic routes.

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