(2S,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanenitrile

≥95%

Reagent Code: #70863
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CAS Number 241479-74-3

science Other reagents with same CAS 241479-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.26 g/mol
Formula C₁₃H₁₂F₂N₄O
badge Registry Numbers
MDL Number MFCD28411477
thermostat Physical Properties
Boiling Point 522.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of antifungal agents. Its structure, featuring a triazole ring, is crucial for its role in inhibiting fungal enzymes, particularly those involved in ergosterol biosynthesis, which is essential for fungal cell membrane integrity. The compound's stereochemistry and functional groups enhance its binding affinity to target enzymes, making it a valuable component in developing potent antifungal drugs. It is often incorporated into formulations aimed at treating systemic fungal infections, particularly those resistant to conventional therapies. Additionally, its unique chemical properties are being explored for potential applications in designing novel therapeutic agents targeting other microbial pathogens.

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Test Parameter Specification
Appearance Conforms to Structure
Purity (%) 95-100
Or[Α] (C=1.3 /100Ml MeOH)(°) -37.5--25

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,241.00
inventory 250mg
10-20 days ฿981.00
inventory 5g
10-20 days ฿7,830.00

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(2S,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanenitrile
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of antifungal agents. Its structure, featuring a triazole ring, is crucial for its role in inhibiting fungal enzymes, particularly those involved in ergosterol biosynthesis, which is essential for fungal cell membrane integrity. The compound's stereochemistry and functional groups enhance its binding affinity to target enzymes, making it a valuable component in developing potent antifungal drugs. It is often incorporated into formulations aimed at treating systemic fungal infections, particularly those resistant to conventional therapies. Additionally, its unique chemical properties are being explored for potential applications in designing novel therapeutic agents targeting other microbial pathogens.
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