N-(4-Hydroxyphenyl)methanesulfonamide

≥98%

Reagent Code: #219502
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CAS Number 51767-39-6

science Other reagents with same CAS 51767-39-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.22 g/mol
Formula C₇H₉NO₃S
badge Registry Numbers
MDL Number MFCD00720883
thermostat Physical Properties
Melting Point 154-156 °C
Boiling Point 357.3 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory agents. It serves as a building block in the preparation of selective COX-2 inhibitors. Also employed in the production of dyes and functional materials due to its sulfonamide and phenolic groups, which allow for diverse chemical modifications. Its structure supports use in research related to drug design and optimization of bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,000.00
inventory 250mg
10-20 days ฿1,480.00
inventory 1g
10-20 days ฿3,470.00
inventory 5g
10-20 days ฿12,480.00
N-(4-Hydroxyphenyl)methanesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory agents. It serves as a building block in the preparation of selective COX-2 inhibitors. Also employed in the production of dyes and functional materials due to its sulfonamide and phenolic groups, which allow for diverse chemical modifications. Its structure supports use in research related to drug design and optimization of bioactive molecules.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory agents. It serves as a building block in the preparation of selective COX-2 inhibitors. Also employed in the production of dyes and functional materials due to its sulfonamide and phenolic groups, which allow for diverse chemical modifications. Its structure supports use in research related to drug design and optimization of bioactive molecules.

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