3-Thiophenecarboxaldehyde

98%

Reagent Code: #239921
label
Alias 3-thiophene formaldehyde;thiophene-3-formaldehyde,3-thiophene
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CAS Number 498-62-4

science Other reagents with same CAS 498-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 112.15 g/mol
Formula C₅H₄OS
badge Registry Numbers
EC Number 207-865-5
MDL Number MFCD00005466
thermostat Physical Properties
Melting Point -30 °C
Boiling Point 194-196 °C(lit.)
inventory_2 Storage & Handling
Density 1.28 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other biologically active compounds. It serves as a building block in organic reactions, especially in the development of thiophene-based derivatives for use in agrochemicals and dyes. Its aldehyde functional group allows for easy modification, making it valuable in the preparation of ligands for catalysis and in the fabrication of conductive polymers for electronic materials. Also employed in the manufacture of specialty chemicals requiring aromatic heterocyclic structures with sulfur functionality.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿990.00
inventory 100g
10-20 days ฿3,880.00
inventory 500g
10-20 days ฿18,640.00

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3-Thiophenecarboxaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other biologically active compounds. It serves as a building block in organic reactions, especially in the development of thiophene-based derivatives for use in agrochemicals and dyes. Its aldehyde functional group allows for easy modification, making it valuable in the preparation of ligands for catalysis and in the fabrication of conductive polymers for electronic materials. Also em

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other biologically active compounds. It serves as a building block in organic reactions, especially in the development of thiophene-based derivatives for use in agrochemicals and dyes. Its aldehyde functional group allows for easy modification, making it valuable in the preparation of ligands for catalysis and in the fabrication of conductive polymers for electronic materials. Also employed in the manufacture of specialty chemicals requiring aromatic heterocyclic structures with sulfur functionality.

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