2,5-Dimethylbenzoyl chloride

97%

Reagent Code: #179170
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CAS Number 22328-43-4

science Other reagents with same CAS 22328-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.62 g/mol
Formula C₉H₉ClO
badge Registry Numbers
MDL Number MFCD00045218
thermostat Physical Properties
Boiling Point 239.3±9.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.136±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in acylation reactions to form esters and amides, making it valuable in the production of active pharmaceutical ingredients (APIs). Its aromatic structure with methyl substituents enhances reactivity and selectivity in certain coupling reactions. Also employed in the preparation of specialty polymers and dyes where controlled substitution patterns are required. Due to its reactivity, it is handled under anhydrous conditions and used in controlled environments to ensure safety and product purity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,630.00
inventory 5g
10-20 days ฿20,590.00
inventory 25g
10-20 days ฿47,190.00

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2,5-Dimethylbenzoyl chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in acylation reactions to form esters and amides, making it valuable in the production of active pharmaceutical ingredients (APIs). Its aromatic structure with methyl substituents enhances reactivity and selectivity in certain coupling reactions. Also employed in the preparation of specialty polymers and dyes where controlled substitution patterns are required. Due to its

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in acylation reactions to form esters and amides, making it valuable in the production of active pharmaceutical ingredients (APIs). Its aromatic structure with methyl substituents enhances reactivity and selectivity in certain coupling reactions. Also employed in the preparation of specialty polymers and dyes where controlled substitution patterns are required. Due to its reactivity, it is handled under anhydrous conditions and used in controlled environments to ensure safety and product purity.

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