2-Thiopheneacetyl chloride

98%

Reagent Code: #239781
label
Alias 2-thiophene acetyl chloride;thiophene-2-chlorine acetate
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CAS Number 39098-97-0

science Other reagents with same CAS 39098-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.62 g/mol
Formula C₆H₅ClOS
badge Registry Numbers
EC Number 254-290-0
MDL Number MFCD00005456
thermostat Physical Properties
Boiling Point 105-106 °C22 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.303 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of the 2-thiopheneacetyl group into larger molecules, making it valuable in the development of active ingredients in drugs, particularly those targeting central nervous system disorders and anti-inflammatory agents. It is also employed in the preparation of specialty polymers and ligands for catalysis due to the thiophene ring’s electron-rich nature. Careful handling is required due to its moisture sensitivity and corrosive properties.

format_list_bulleted Product Specification

Test Parameter Specification
Free Acid 0-2%
Purity (Titration with AgNO3) 97.5-102.5%
Refractive Index (N20/D) 1.55-1.552
Appearance colorless to pale brown liquid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿630.00
inventory 500g
10-20 days ฿9,260.00
inventory 100g
10-20 days ฿1,960.00
2-Thiopheneacetyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of the 2-thiopheneacetyl group into larger molecules, making it valuable in the development of active ingredients in drugs, particularly those targeting central nervous system disorders and anti-inflammatory agents. It is also employed in the preparation of specialty polymers and ligands for catalysis due to the thiophene ring’s electron-rich nature. Careful handling is requ

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of the 2-thiopheneacetyl group into larger molecules, making it valuable in the development of active ingredients in drugs, particularly those targeting central nervous system disorders and anti-inflammatory agents. It is also employed in the preparation of specialty polymers and ligands for catalysis due to the thiophene ring’s electron-rich nature. Careful handling is required due to its moisture sensitivity and corrosive properties.

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