5-Bromo-3-methylthiophene-2-carbaldehyde

≥95%

Reagent Code: #172976
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CAS Number 38239-46-2

science Other reagents with same CAS 38239-46-2

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Weight 205.07 g/mol
Formula C₆H₅BrOS
badge Registry Numbers
MDL Number MFCD10000783
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and condensation processes, making it valuable in medicinal chemistry for constructing heterocyclic compounds with potential antitumor, antimicrobial, or anti-inflammatory activities. Also employed in the preparation of organic semiconductors and functional materials due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,790.00
inventory 1g
10-20 days ฿12,000.00

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5-Bromo-3-methylthiophene-2-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and condensation processes, making it valuable in medicinal chemistry for constructing heterocyclic compounds with potential antitumor, antimicrobial, or anti-inflammatory activities. Also employed in the preparation of organic semicon

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its aldehyde and bromo functional groups allow for versatile chemical transformations, such as cross-coupling reactions and condensation processes, making it valuable in medicinal chemistry for constructing heterocyclic compounds with potential antitumor, antimicrobial, or anti-inflammatory activities. Also employed in the preparation of organic semiconductors and functional materials due to the electron-rich nature of the thiophene ring.

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