Methyl (2-nitrophenyl)sulfane

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Reagent Code: #206489
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CAS Number 3058-47-7

science Other reagents with same CAS 3058-47-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.2 g/mol
Formula C₇H₇NO₂S
badge Registry Numbers
MDL Number MFCD03094691
thermostat Physical Properties
Boiling Point 264.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through reduction of the nitro group or substitution of the sulfide moiety. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules where the nitroaryl thioether scaffold is required. Also finds use in research settings for studying sulfur-containing aromatic systems and their reactivity in cross-coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,090.00
inventory 100mg
10-20 days ฿3,730.00
inventory 250mg
10-20 days ฿6,900.00
inventory 1g
10-20 days ฿15,600.00
inventory 5g
10-20 days ฿47,000.00

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Methyl (2-nitrophenyl)sulfane
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through reduction of the nitro group or substitution of the sulfide moiety. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules where the nitroaryl thioether scaffold is required. Also finds use in research settings for studying sulfur-containing aromatic systems and their reactivity in cross-coupl

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through reduction of the nitro group or substitution of the sulfide moiety. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules where the nitroaryl thioether scaffold is required. Also finds use in research settings for studying sulfur-containing aromatic systems and their reactivity in cross-coupling reactions.

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