2,4-Dichloro-5-chloromethyl-pyrimidine

95%

Reagent Code: #177262
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CAS Number 7627-38-5

science Other reagents with same CAS 7627-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.45 g/mol
Formula C₅H₃Cl₃N₂
badge Registry Numbers
MDL Number MFCD10697639
thermostat Physical Properties
Melting Point 63-64 °C
Boiling Point 90-100 °C(Press: 0.001 Torr)
inventory_2 Storage & Handling
Density 1.548±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and plant growth regulators. Its reactivity allows for the introduction of pyrimidine-based functional groups into larger molecules, enhancing their biological activity. Also employed in the development of pharmaceuticals where chlorinated pyrimidine scaffolds are needed for drug design, especially in antiviral and anticancer agents. Commonly utilized in research laboratories for constructing complex heterocyclic systems through nucleophilic substitution or cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿730.00
inventory 250mg
10-20 days ฿1,170.00
inventory 1g
10-20 days ฿3,140.00

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2,4-Dichloro-5-chloromethyl-pyrimidine
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and plant growth regulators. Its reactivity allows for the introduction of pyrimidine-based functional groups into larger molecules, enhancing their biological activity. Also employed in the development of pharmaceuticals where chlorinated pyrimidine scaffolds are needed for drug design, especially in antiviral and anticancer agents. Commonly utilized in research laboratories for constructing comple

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and plant growth regulators. Its reactivity allows for the introduction of pyrimidine-based functional groups into larger molecules, enhancing their biological activity. Also employed in the development of pharmaceuticals where chlorinated pyrimidine scaffolds are needed for drug design, especially in antiviral and anticancer agents. Commonly utilized in research laboratories for constructing complex heterocyclic systems through nucleophilic substitution or cross-coupling reactions.

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