4-Nitrothioanisole

98%

Reagent Code: #216650
label
Alias 4-Nitroxanis sulfide
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CAS Number 701-57-5

science Other reagents with same CAS 701-57-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.2 g/mol
Formula O₂NC₆H₄SCH₃
badge Registry Numbers
MDL Number MFCD00010868
thermostat Physical Properties
Melting Point 66-69 °C(lit.)
Boiling Point 140 °C / 2mmHg
inventory_2 Storage & Handling
Storage Room temperature

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 derivatives and other sulfur-containing compounds. Its nitro group allows for further functionalization through reduction to an amine, enabling coupling reactions in the synthesis of dyes and functional materials. Also employed in research for studying nucleophilic aromatic substitution reactions due to the electron-withdrawing nature of the nitro group enhancing reactivity at the aromatic ring.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿400.00
25g
10-20 days ฿1,140.00
100g
10-20 days ฿4,200.00
500g
10-20 days ฿14,950.00
4-Nitrothioanisole
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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 derivatives and other sulfur-containing compounds. Its nitro group allows for further functionalization through reduction to an amine, enabling coupling reactions in the synthesis of dyes and functional materials. Also employed in research for studying nucleophilic aromatic substitution reactions due to the electron-withdrawing

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 derivatives and other sulfur-containing compounds. Its nitro group allows for further functionalization through reduction to an amine, enabling coupling reactions in the synthesis of dyes and functional materials. Also employed in research for studying nucleophilic aromatic substitution reactions due to the electron-withdrawing nature of the nitro group enhancing reactivity at the aromatic ring.

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