5-Amino-4,6-dichloro-2-methylpyrimidine

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Reagent Code: #135293
label
Alias 2-methyl-4,6-dichloro-5-aminopyrimidine; 2-methyl-5-amino-4,6-dichloropyrimidine
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CAS Number 39906-04-2

science Other reagents with same CAS 39906-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.02 g/mol
Formula C₅H₅Cl₂N₃
badge Registry Numbers
MDL Number MFCD00194053
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization in the development of chlorinated pyrimidine derivatives, which exhibit biological activity in crop protection. Also employed in the preparation of pharmaceuticals where pyrimidine scaffolds are needed, especially in antiviral and antimicrobial agents. Commonly utilized in research settings for building more complex heterocyclic systems through nucleophilic substitution or condensation reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿144.00
inventory 5g
10-20 days ฿180.00
inventory 25g
10-20 days ฿1,260.00

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5-Amino-4,6-dichloro-2-methylpyrimidine
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization in the development of chlorinated pyrimidine derivatives, which exhibit biological activity in crop protection. Also employed in the preparation of pharmaceuticals where pyrimidine scaffolds are needed, especially in antiviral and antimicrobial agents. Commonly utilized in research settings for building more complex heterocyclic systems thro

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization in the development of chlorinated pyrimidine derivatives, which exhibit biological activity in crop protection. Also employed in the preparation of pharmaceuticals where pyrimidine scaffolds are needed, especially in antiviral and antimicrobial agents. Commonly utilized in research settings for building more complex heterocyclic systems through nucleophilic substitution or condensation reactions.

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