5-amino-1,6-dihydro-6-thioxopyridine-3-carboxylicacid

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Reagent Code: #48396
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CAS Number 935687-88-0

science Other reagents with same CAS 935687-88-0

blur_circular Chemical Specifications

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Weight 170.19 g/mol
Formula C₆H₆N₂O₂S
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound, 5-amino-1,6-dihydro-6-thioxopyridine-3-carboxylic acid, is a specialty chemical intermediate primarily used in medicinal chemistry for the synthesis of pharmaceuticals. It plays a key role in developing antimicrobial agents against bacterial infections, anti-inflammatory drugs, and potential anti-cancer therapeutics. The amino group at position 5, thioxo group at position 6, and carboxylic acid at position 3 provide versatility in organic reactions, enabling the formation of complex heterocyclic structures with diverse biological activities. It serves as a building block for creating molecules that inhibit bacterial growth and exhibit therapeutic effects.

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inventory 1g
10-20 days ฿43,200.00

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5-amino-1,6-dihydro-6-thioxopyridine-3-carboxylicacid
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This compound, 5-amino-1,6-dihydro-6-thioxopyridine-3-carboxylic acid, is a specialty chemical intermediate primarily used in medicinal chemistry for the synthesis of pharmaceuticals. It plays a key role in developing antimicrobial agents against bacterial infections, anti-inflammatory drugs, and potential anti-cancer therapeutics. The amino group at position 5, thioxo group at position 6, and carboxylic acid at position 3 provide versatility in organic reactions, enabling the formation of complex hetero

This compound, 5-amino-1,6-dihydro-6-thioxopyridine-3-carboxylic acid, is a specialty chemical intermediate primarily used in medicinal chemistry for the synthesis of pharmaceuticals. It plays a key role in developing antimicrobial agents against bacterial infections, anti-inflammatory drugs, and potential anti-cancer therapeutics. The amino group at position 5, thioxo group at position 6, and carboxylic acid at position 3 provide versatility in organic reactions, enabling the formation of complex heterocyclic structures with diverse biological activities. It serves as a building block for creating molecules that inhibit bacterial growth and exhibit therapeutic effects.

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