2,5-Dichlorobenzophenone

≥97%

Reagent Code: #172458
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CAS Number 16611-67-9

science Other reagents with same CAS 16611-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.11 g/mol
Formula C₁₃H₈Cl₂O
badge Registry Numbers
MDL Number MFCD00079746
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) and antihistamines. It serves as a building block in organic reactions where a benzophenone scaffold with specific halogen substitutions is required. Its chloro groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for developing active drug compounds. Also utilized in the preparation of photoinitiators for UV-curable coatings and polymers due to its ability to absorb ultraviolet light and generate free radicals.

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿1,010.00
inventory 500g
10-20 days ฿4,480.00
inventory 1kg
10-20 days ฿8,370.00

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2,5-Dichlorobenzophenone
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) and antihistamines. It serves as a building block in organic reactions where a benzophenone scaffold with specific halogen substitutions is required. Its chloro groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for developing active drug compounds. Also utilized in the preparation of phot

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) and antihistamines. It serves as a building block in organic reactions where a benzophenone scaffold with specific halogen substitutions is required. Its chloro groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for developing active drug compounds. Also utilized in the preparation of photoinitiators for UV-curable coatings and polymers due to its ability to absorb ultraviolet light and generate free radicals.

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