3-(methoxymethyl)-4-methyl-1H-1,2,4-triazole-5-thione

95%

Reagent Code: #196261
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CAS Number 113657-01-5

science Other reagents with same CAS 113657-01-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.21 g/mol
Formula C₅H₉N₃OS
badge Registry Numbers
MDL Number MFCD03945579
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of triazole-based antifungal agents. It exhibits strong coordination ability with metal ions, making it useful in the development of metal-organic frameworks (MOFs) for catalytic applications. Also employed in the pharmaceutical industry for designing bioactive molecules with antimicrobial and antiviral properties. Its thione group enhances reactivity in heterocyclic transformations, supporting its role in creating complex medicinal compounds.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿76,240.00
inventory 1g
10-20 days ฿26,340.00

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3-(methoxymethyl)-4-methyl-1H-1,2,4-triazole-5-thione
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Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of triazole-based antifungal agents. It exhibits strong coordination ability with metal ions, making it useful in the development of metal-organic frameworks (MOFs) for catalytic applications. Also employed in the pharmaceutical industry for designing bioactive molecules with antimicrobial and antiviral properties. Its thione group enhances reactivity in heterocyclic transformations, supporting its role

Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of triazole-based antifungal agents. It exhibits strong coordination ability with metal ions, making it useful in the development of metal-organic frameworks (MOFs) for catalytic applications. Also employed in the pharmaceutical industry for designing bioactive molecules with antimicrobial and antiviral properties. Its thione group enhances reactivity in heterocyclic transformations, supporting its role in creating complex medicinal compounds.

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