Pyrrole-2-carboxaldehyde

98%

Reagent Code: #224827
label
Alias 2-pyrrole formaldehyde; 2-aldehyde pyrrole; 2-formylpyrrole
fingerprint
CAS Number 1003-29-8

science Other reagents with same CAS 1003-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 95.10 g/mol
Formula C₅H₅NO
badge Registry Numbers
EC Number 213-705-5
MDL Number MFCD00005217
thermostat Physical Properties
Melting Point 43-46 °C(lit.)
Boiling Point 217-219 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of pyrrole-based bioactive compounds. It serves as a building block in the development of antifungal, antibacterial, and anticancer agents due to its reactive aldehyde group and aromatic heterocyclic structure. Also employed in the preparation of dyes, pigments, and functional materials such as conductive polymers and sensors. Its ability to form Schiff bases makes it valuable in coordination chemistry and catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿340.00
5g
10-20 days ฿460.00
25g
10-20 days ฿1,550.00
100g
10-20 days ฿5,800.00
500g
10-20 days ฿24,050.00
Pyrrole-2-carboxaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of pyrrole-based bioactive compounds. It serves as a building block in the development of antifungal, antibacterial, and anticancer agents due to its reactive aldehyde group and aromatic heterocyclic structure. Also employed in the preparation of dyes, pigments, and functional materials such as conductive polymers and sensors. Its ability to form Schiff bases makes it valuable in coordination

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of pyrrole-based bioactive compounds. It serves as a building block in the development of antifungal, antibacterial, and anticancer agents due to its reactive aldehyde group and aromatic heterocyclic structure. Also employed in the preparation of dyes, pigments, and functional materials such as conductive polymers and sensors. Its ability to form Schiff bases makes it valuable in coordination chemistry and catalysis.

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