Benzyl Methyl Sulfide

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Reagent Code: #147025
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CAS Number 766-92-7

science Other reagents with same CAS 766-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.23 g/mol
Formula C₈H₁₀S
badge Registry Numbers
MDL Number MFCD00008563
thermostat Physical Properties
Boiling Point 200°C(lit.)
inventory_2 Storage & Handling
Density 1.03g/mL
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 formation of more complex sulfur-containing compounds. Due to its sulfide functionality, it participates in oxidation reactions to produce sulfoxides or sulfones, which are valuable motifs in drug design. Also employed in fragrance chemistry, contributing to the development of sulfur-based aroma compounds with onion-like or savory notes, useful in flavor formulations. Its reactivity makes it suitable for use in research laboratories for exploring new synthetic pathways and catalytic transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿410.00
inventory 25g
10-20 days ฿1,550.00
inventory 100g
10-20 days ฿5,250.00
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Benzyl Methyl Sulfide
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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 formation of more complex sulfur-containing compounds. Due to its sulfide functionality, it participates in oxidation reactions to produce sulfoxides or sulfones, which are valuable motifs in drug design. Also employed in fragrance chemistry, contributing to the development of sulfur-based aroma compounds with onion-like or savory notes, useful in flavor

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of more complex sulfur-containing compounds. Due to its sulfide functionality, it participates in oxidation reactions to produce sulfoxides or sulfones, which are valuable motifs in drug design. Also employed in fragrance chemistry, contributing to the development of sulfur-based aroma compounds with onion-like or savory notes, useful in flavor formulations. Its reactivity makes it suitable for use in research laboratories for exploring new synthetic pathways and catalytic transformations.

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