4-Isopropylbenzoyl chloride

≥95%

Reagent Code: #200826
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CAS Number 21900-62-9

science Other reagents with same CAS 21900-62-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.65 g/mol
Formula C₁₀H₁₁ClO
badge Registry Numbers
MDL Number MFCD03424703
inventory_2 Storage & Handling
Density 1.100±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as an acylating agent in organic reactions, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and related derivatives. Its reactivity allows for the introduction of the 4-isopropylbenzoyl group into various compounds, enhancing lipophilicity and influencing biological activity. Also employed in the preparation of liquid crystals and functional materials where specific aromatic ketone structures are required. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions in controlled environments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,910.00
inventory 1g
10-20 days ฿5,410.00
inventory 5g
10-20 days ฿22,100.00
4-Isopropylbenzoyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as an acylating agent in organic reactions, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and related derivatives. Its reactivity allows for the introduction of the 4-isopropylbenzoyl group into various compounds, enhancing lipophilicity and influencing biological activity. Also employed in the preparation of liquid crystals and functional materials where

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as an acylating agent in organic reactions, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and related derivatives. Its reactivity allows for the introduction of the 4-isopropylbenzoyl group into various compounds, enhancing lipophilicity and influencing biological activity. Also employed in the preparation of liquid crystals and functional materials where specific aromatic ketone structures are required. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions in controlled environments.

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