4-(Bromomethyl)benzophenone

>96%

Reagent Code: #144760
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CAS Number 32752-54-8

science Other reagents with same CAS 32752-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.15 g/mol
Formula C₁₄H₁₁BrO
badge Registry Numbers
MDL Number MFCD00092076
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. It enables the introduction of benzophenone-linked benzyl groups through the reactive bromomethyl functionality. Commonly employed in the preparation of photoinitiators for polymer chemistry, where it participates in radical reactions upon UV exposure. Also utilized in the synthesis of functionalized ligands for coordination chemistry and in the development of specialty resins due to its ability to form covalent bonds with nucleophiles like amines and thiols. Its photoreactive nature makes it suitable for crosslinking applications in coatings and adhesives.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,450.00
5g
10-20 days ฿4,610.00
25g
10-20 days ฿16,420.00
100g
10-20 days ฿50,030.00
4-(Bromomethyl)benzophenone
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Used as a key intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It enables the introduction of benzophenone-linked benzyl groups through the reactive bromomethyl functionality. Commonly employed in the preparation of photoinitiators for polymer chemistry, where it participates in radical reactions upon UV exposure. Also utilized in the synthesis of functionalized ligands for coordination chemistry and in the development of specialty resins due to its ability to form co

Used as a key intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It enables the introduction of benzophenone-linked benzyl groups through the reactive bromomethyl functionality. Commonly employed in the preparation of photoinitiators for polymer chemistry, where it participates in radical reactions upon UV exposure. Also utilized in the synthesis of functionalized ligands for coordination chemistry and in the development of specialty resins due to its ability to form covalent bonds with nucleophiles like amines and thiols. Its photoreactive nature makes it suitable for crosslinking applications in coatings and adhesives.

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