3'-Methylbiphenyl-4-sulfonyl chloride

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Reagent Code: #214208
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CAS Number 186551-47-3

science Other reagents with same CAS 186551-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.74 g/mol
Formula C₁₃H₁₁ClO₂S
badge Registry Numbers
MDL Number MFCD06409269
thermostat Physical Properties
Melting Point 69-72 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its sulfonyl chloride functional group allows for easy attachment to other molecules, making it valuable in constructing complex drug structures. It is also employed in the preparation of liquid crystals and agrochemicals due to its stable biphenyl backbone and reactivity profile. Commonly used in organic synthesis for introducing the 3'-methylbiphenyl-4-ylsulfonyl moiety into target compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿8,010.00
3'-Methylbiphenyl-4-sulfonyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its sulfonyl chloride functional group allows for easy attachment to other molecules, making it valuable in constructing complex drug structures. It is also employed in the preparation of liquid crystals and agrochemicals due to its stable biphenyl backbone and reactivity profile. Commonly used in organic synthesis for intro

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its sulfonyl chloride functional group allows for easy attachment to other molecules, making it valuable in constructing complex drug structures. It is also employed in the preparation of liquid crystals and agrochemicals due to its stable biphenyl backbone and reactivity profile. Commonly used in organic synthesis for introducing the 3'-methylbiphenyl-4-ylsulfonyl moiety into target compounds.

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