N-Phenylmethanesulfonamide

98%

Reagent Code: #217227
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CAS Number 1197-22-4

science Other reagents with same CAS 1197-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.22 g/mol
Formula C₇H₉NO₂S
badge Registry Numbers
MDL Number MFCD00043782
thermostat Physical Properties
Melting Point 93-97°C
Boiling Point 284°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the development of sulfonamide-based bioactive compounds due to its stability and reactivity. Commonly employed in the synthesis of herbicides and fungicides, it contributes to the structural framework that enhances biological activity. Also utilized in research settings for the development of new synthetic routes and catalytic processes. Its ability to act as a directing group in C–H activation reactions makes it valuable in advanced organic transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿510.00
inventory 25g
10-20 days ฿2,340.00
inventory 100g
10-20 days ฿9,120.00

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N-Phenylmethanesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the development of sulfonamide-based bioactive compounds due to its stability and reactivity. Commonly employed in the synthesis of herbicides and fungicides, it contributes to the structural framework that enhances biological activity. Also utilized in research settings for the development of new synthetic routes and catalytic processes. Its ability to act

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the development of sulfonamide-based bioactive compounds due to its stability and reactivity. Commonly employed in the synthesis of herbicides and fungicides, it contributes to the structural framework that enhances biological activity. Also utilized in research settings for the development of new synthetic routes and catalytic processes. Its ability to act as a directing group in C–H activation reactions makes it valuable in advanced organic transformations.

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