4-(Methylthio)benzyl chloride

97%

Reagent Code: #204753
label
Alias 4-methylthiochlorobenzyl
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CAS Number 874-87-3

science Other reagents with same CAS 874-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.68 g/mol
Formula C₈H₉ClS
badge Registry Numbers
EC Number 212-870-0
MDL Number MFCD00270118
thermostat Physical Properties
Boiling Point 116°C 8mm
inventory_2 Storage & Handling
Density 1.170 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of sulfonamide and thioether derivatives. Its reactivity allows for the introduction of the 4-(methylthio)benzyl group into larger molecules, enhancing lipophilicity and influencing biological activity. Commonly employed in the development of herbicides and fungicides due to the stability and bioavailability imparted by the methylthio and benzyl moieties. Also utilized in the production of specialty polymers and as a building block in organic synthesis for creating complex aromatic compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿950.00
inventory 5g
10-20 days ฿4,180.00
inventory 25g
10-20 days ฿17,680.00
inventory 100g
10-20 days ฿47,720.00

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4-(Methylthio)benzyl chloride
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of sulfonamide and thioether derivatives. Its reactivity allows for the introduction of the 4-(methylthio)benzyl group into larger molecules, enhancing lipophilicity and influencing biological activity. Commonly employed in the development of herbicides and fungicides due to the stability and bioavailability imparted by the methylthio and benzyl moieties. Also utilized in the production of specialt
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of sulfonamide and thioether derivatives. Its reactivity allows for the introduction of the 4-(methylthio)benzyl group into larger molecules, enhancing lipophilicity and influencing biological activity. Commonly employed in the development of herbicides and fungicides due to the stability and bioavailability imparted by the methylthio and benzyl moieties. Also utilized in the production of specialty polymers and as a building block in organic synthesis for creating complex aromatic compounds.
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