3-(Trifluoromethoxy)benzohydrazide

97%

Reagent Code: #238392
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CAS Number 321195-88-4

science Other reagents with same CAS 321195-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.15 g/mol
Formula C₈H₇F₃N₂O₂
badge Registry Numbers
MDL Number MFCD03425698
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to the presence of the trifluoromethoxy group, which enhances lipophilicity and metabolic stability. Also employed in the preparation of heterocyclic compounds such as 1,3,4-oxadiazoles and 1,2,4-triazoles, which are common scaffolds in bioactive molecules. Its hydrazide functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing libraries of compounds in drug discovery programs. Shows potential in research focused on novel anti-inflammatory and antimicrobial agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,160.00
inventory 250mg
10-20 days ฿1,880.00
inventory 1g
10-20 days ฿4,940.00
3-(Trifluoromethoxy)benzohydrazide
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to the presence of the trifluoromethoxy group, which enhances lipophilicity and metabolic stability. Also employed in the preparation of heterocyclic compounds such as 1,3,4-oxadiazoles and 1,2,4-triazoles, which are common scaffolds in bioactive molecules. Its hydrazide functionality allows for easy derivatization, making it valuable in medicinal chemistry for c
Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to the presence of the trifluoromethoxy group, which enhances lipophilicity and metabolic stability. Also employed in the preparation of heterocyclic compounds such as 1,3,4-oxadiazoles and 1,2,4-triazoles, which are common scaffolds in bioactive molecules. Its hydrazide functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing libraries of compounds in drug discovery programs. Shows potential in research focused on novel anti-inflammatory and antimicrobial agents.
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