5-iodo-4-methoxy-6-methyl-2-(methylthio)pyrimidine

95%

Reagent Code: #200635
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CAS Number 107166-95-0

science Other reagents with same CAS 107166-95-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.13 g/mol
Formula C₇H₉IN₂OS
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MDL Number MFCD26960810
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective reactivity, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyrimidine core into bioactive molecules. Also utilized in research settings for the design of kinase inhibitors and other targeted therapies due to its ability to mimic natural nucleotide components.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,090.00
inventory 250mg
10-20 days ฿14,040.00
inventory 1g
10-20 days ฿28,080.00
5-iodo-4-methoxy-6-methyl-2-(methylthio)pyrimidine
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective reactivity, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyrimidine core into bioactive molecules. Also utilized in research settings for the design of kinase inhibitors and other targeted therapies due to its ability to mimic natural nucleotide c

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective reactivity, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyrimidine core into bioactive molecules. Also utilized in research settings for the design of kinase inhibitors and other targeted therapies due to its ability to mimic natural nucleotide components.

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