2,4,6-Trimethylbenzyl Chloride

98%

Reagent Code: #240538
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CAS Number 1585-16-6

science Other reagents with same CAS 1585-16-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.66 g/mol
Formula C₁₀H₁₃Cl
badge Registry Numbers
MDL Number MFCD00000901
thermostat Physical Properties
Melting Point 39-42°C (Lit.)
inventory_2 Storage & Handling
Storage 2~8°C, sealed

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. It serves as a building block in the production of certain herbicides and insecticides due to its reactive benzyl chloride group, which readily undergoes nucleophilic substitution. Also employed in the preparation of specialty resins and functionalized aromatic compounds where steric hindrance from the trimethyl groups influences reaction selectivity. Its stability and solubility profile make it suitable for use in controlled organic transformations, particularly in fine chemical manufacturing.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿880.00
inventory 100g
10-20 days ฿3,370.00
inventory 500g
10-20 days ฿16,400.00
2,4,6-Trimethylbenzyl Chloride
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. It serves as a building block in the production of certain herbicides and insecticides due to its reactive benzyl chloride group, which readily undergoes nucleophilic substitution. Also employed in the preparation of specialty resins and functionalized aromatic compounds where steric hindrance from the trimethyl groups influences reaction selectivity. Its stability and solubility profile make it suitable for use in c

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. It serves as a building block in the production of certain herbicides and insecticides due to its reactive benzyl chloride group, which readily undergoes nucleophilic substitution. Also employed in the preparation of specialty resins and functionalized aromatic compounds where steric hindrance from the trimethyl groups influences reaction selectivity. Its stability and solubility profile make it suitable for use in controlled organic transformations, particularly in fine chemical manufacturing.

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