2,3,4,5,6-Pentamethylbenzyl Chloride

98%,GC

Reagent Code: #225475
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CAS Number 484-65-1

science Other reagents with same CAS 484-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.72 g/mol
Formula C₁₂H₁₇Cl
badge Registry Numbers
MDL Number MFCD00000900
thermostat Physical Properties
Melting Point 80-85°C
Boiling Point 140-142°C
inventory_2 Storage & Handling
Density 0.991 g/cm3
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized aromatic derivatives for pharmaceuticals and agrochemicals. Its reactive benzyl chloride group allows for easy substitution, enabling the attachment of various moieties in multi-step syntheses. It is also employed in the development of specialty polymers and ligands for catalysis due to the steric and electronic influence of the pentamethyl-substituted ring. Additionally, it finds use in research settings for studying steric effects on reaction kinetics and selectivity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,680.00
2,3,4,5,6-Pentamethylbenzyl Chloride
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized aromatic derivatives for pharmaceuticals and agrochemicals. Its reactive benzyl chloride group allows for easy substitution, enabling the attachment of various moieties in multi-step syntheses. It is also employed in the development of specialty polymers and ligands for catalysis due to the steric and electronic influence of the pentamethyl-substituted ring. Additionally, it finds use in rese

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized aromatic derivatives for pharmaceuticals and agrochemicals. Its reactive benzyl chloride group allows for easy substitution, enabling the attachment of various moieties in multi-step syntheses. It is also employed in the development of specialty polymers and ligands for catalysis due to the steric and electronic influence of the pentamethyl-substituted ring. Additionally, it finds use in research settings for studying steric effects on reaction kinetics and selectivity.

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