2-Hydrazinyl-5-(trifluoromethyl)benzo[d]thiazole

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Reagent Code: #196408
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CAS Number 80945-79-5

science Other reagents with same CAS 80945-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.21 g/mol
Formula C₈H₆F₃N₃S
badge Registry Numbers
MDL Number MFCD09040770
inventory_2 Storage & Handling
Storage -20°C, preserved from light, inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated heterocyclic compounds for pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. Its hydrazine functionality allows for condensation reactions to form hydrazones and azoles, which are common scaffolds in bioactive molecules. Also employed in the preparation of fluorescent dyes and sensors due to its electron-withdrawing trifluoromethyl group and rigid aromatic structure, enhancing photostability and signal detection in imaging applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿32,580.00
1g
10-20 days ฿75,160.00
100mg
10-20 days ฿17,250.00
2-Hydrazinyl-5-(trifluoromethyl)benzo[d]thiazole
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Used as a key intermediate in the synthesis of fluorinated heterocyclic compounds for pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. Its hydrazine functionality allows for condensation reactions to form hydrazones and azoles, which are common scaffolds in bioactive molecules. Also employed in the preparation of fluorescent dyes and sensors due to its electron-withdrawing trifluoromethyl group and rigid aromatic structure, enhancing photostability and signal detect

Used as a key intermediate in the synthesis of fluorinated heterocyclic compounds for pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. Its hydrazine functionality allows for condensation reactions to form hydrazones and azoles, which are common scaffolds in bioactive molecules. Also employed in the preparation of fluorescent dyes and sensors due to its electron-withdrawing trifluoromethyl group and rigid aromatic structure, enhancing photostability and signal detection in imaging applications.

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