N,N-Dibenzyl-1-phenylmethanesulfonamide

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Reagent Code: #214765
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CAS Number 346727-34-2

science Other reagents with same CAS 346727-34-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.46 g/mol
Formula C₂₁H₂₁NO₂S
badge Registry Numbers
MDL Number MFCD01214392
thermostat Physical Properties
Melting Point 98-99 °C
Boiling Point 533.1±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.218±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block in the preparation of sulfonamide-based drugs, which are known for their antimicrobial and enzyme-inhibiting properties. Its structure allows for selective modifications, making it valuable in medicinal chemistry research for designing protease inhibitors and other bioactive molecules. Also employed in the study of reaction mechanisms involving sulfonamides due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,590.00
inventory 500mg
10-20 days ฿3,430.00

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N,N-Dibenzyl-1-phenylmethanesulfonamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block in the preparation of sulfonamide-based drugs, which are known for their antimicrobial and enzyme-inhibiting properties. Its structure allows for selective modifications, making it valuable in medicinal chemistry research for designing protease inhibitors and other bioactive molecules. Also employed in the study of reaction mechanisms involving sulfonamides due to its s

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block in the preparation of sulfonamide-based drugs, which are known for their antimicrobial and enzyme-inhibiting properties. Its structure allows for selective modifications, making it valuable in medicinal chemistry research for designing protease inhibitors and other bioactive molecules. Also employed in the study of reaction mechanisms involving sulfonamides due to its stability and reactivity profile.

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