4-Amino-2,6-dichloropyrimidine

95%

Reagent Code: #135404
label
Alias 2,6-dichloro-4-aminopyrimidine;
fingerprint
CAS Number 10132-07-7

science Other reagents with same CAS 10132-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.99 g/mol
Formula C₄H₃Cl₂N₃
badge Registry Numbers
EC Number 233-369-3
MDL Number MFCD00038015
thermostat Physical Properties
Melting Point 258-267°C
Boiling Point 323.5ºC
inventory_2 Storage & Handling
Density 1.606 g/cm3
Storage 2~8°C

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of sulfonylurea herbicides. It plays a key role in creating active compounds that inhibit plant growth by targeting specific enzymes in weeds. Also employed in the development of certain antimicrobial agents and in research for novel drug candidates due to its reactive amino and chloro groups, which allow for further chemical modifications. Commonly utilized in heterocyclic chemistry for building more complex pyrimidine-based structures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿709.50
inventory 100g
10-20 days ฿4,590.00
inventory 500g
10-20 days ฿12,369.50
4-Amino-2,6-dichloropyrimidine
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of sulfonylurea herbicides. It plays a key role in creating active compounds that inhibit plant growth by targeting specific enzymes in weeds. Also employed in the development of certain antimicrobial agents and in research for novel drug candidates due to its reactive amino and chloro groups, which allow for further chemical modifications. Commonly utilized in heterocyclic chemistry for building

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of sulfonylurea herbicides. It plays a key role in creating active compounds that inhibit plant growth by targeting specific enzymes in weeds. Also employed in the development of certain antimicrobial agents and in research for novel drug candidates due to its reactive amino and chloro groups, which allow for further chemical modifications. Commonly utilized in heterocyclic chemistry for building more complex pyrimidine-based structures.

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