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

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Reagent Code: #135740
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CAS Number 7153-13-1

science Other reagents with same CAS 7153-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.02 g/mol
Formula C₅H₅Cl₂N₃
thermostat Physical Properties
Boiling Point 354.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to create active ingredients that target specific enzyme pathways in weeds. Also employed in the development of pharmaceuticals, where it serves as a building block for compounds with potential antimicrobial or antiviral properties. Commonly utilized in research settings for designing novel heterocyclic compounds due to its reactive amino and chloro groups, which facilitate coupling reactions and nucleophilic substitutions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿640.00
inventory 1g
10-20 days ฿870.00
inventory 5g
10-20 days ฿4,350.00
inventory 25g
10-20 days ฿17,320.00

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2-Amino-4,6-dichloro-5-methylpyrimidine
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Used as an intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to create active ingredients that target specific enzyme pathways in weeds. Also employed in the development of pharmaceuticals, where it serves as a building block for compounds with potential antimicrobial or antiviral properties. Commonly utilized in research settings for designing novel heterocyclic compounds due to its reactive amino and c

Used as an intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to create active ingredients that target specific enzyme pathways in weeds. Also employed in the development of pharmaceuticals, where it serves as a building block for compounds with potential antimicrobial or antiviral properties. Commonly utilized in research settings for designing novel heterocyclic compounds due to its reactive amino and chloro groups, which facilitate coupling reactions and nucleophilic substitutions.

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