2,3-Dimethylbenzoyl chloride

96%

Reagent Code: #179356
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CAS Number 21900-46-9

science Other reagents with same CAS 21900-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.62 g/mol
Formula C₉H₉ClO
badge Registry Numbers
MDL Number MFCD00045217
thermostat Physical Properties
Melting Point 2 °C
Boiling Point 122 °C
inventory_2 Storage & Handling
Density 1.136±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in Friedel-Crafts acylation and other acylation reactions to introduce the 2,3-dimethylbenzoyl group into target molecules. Commonly employed in the preparation of ketones, esters, and amides with specific aromatic substitution patterns. Its reactivity makes it valuable for constructing complex organic frameworks in active pharmaceutical ingredients (APIs) and functional materials. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿3,890.00
inventory 5g
10-20 days ฿13,610.00

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2,3-Dimethylbenzoyl chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in Friedel-Crafts acylation and other acylation reactions to introduce the 2,3-dimethylbenzoyl group into target molecules. Commonly employed in the preparation of ketones, esters, and amides with specific aromatic substitution patterns. Its reactivity makes it valuable for constructing complex organic frameworks in active pharmaceutical ingredients (APIs) and functional m

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It participates in Friedel-Crafts acylation and other acylation reactions to introduce the 2,3-dimethylbenzoyl group into target molecules. Commonly employed in the preparation of ketones, esters, and amides with specific aromatic substitution patterns. Its reactivity makes it valuable for constructing complex organic frameworks in active pharmaceutical ingredients (APIs) and functional materials. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions.

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