(2,4-Diphenylthiazol-5-yl)methanamine hydrochloride

98%

Reagent Code: #180348
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CAS Number 879896-44-3

science Other reagents with same CAS 879896-44-3

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Weight 302.82 g/mol
Formula C₁₆H₁₅ClN₂S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as a key intermediate for pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its amine functionality allows for easy derivatization, making it valuable in constructing drug-like scaffolds. Commonly employed in the preparation of thiazole-based derivatives with potential antimicrobial, anti-inflammatory, or anticancer activities. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to the stability and reactivity of the thiazole core. Suitable for coupling reactions in peptide-like synthesis and combinatorial chemistry.

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inventory 1g
10-20 days ฿18,550.00

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(2,4-Diphenylthiazol-5-yl)methanamine hydrochloride
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Used in organic synthesis as a key intermediate for pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its amine functionality allows for easy derivatization, making it valuable in constructing drug-like scaffolds. Commonly employed in the preparation of thiazole-based derivatives with potential antimicrobial, anti-inflammatory, or anticancer activities. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to the
Used in organic synthesis as a key intermediate for pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its amine functionality allows for easy derivatization, making it valuable in constructing drug-like scaffolds. Commonly employed in the preparation of thiazole-based derivatives with potential antimicrobial, anti-inflammatory, or anticancer activities. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to the stability and reactivity of the thiazole core. Suitable for coupling reactions in peptide-like synthesis and combinatorial chemistry.
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