2-Chloro-3-nitropyrazine

98%

Reagent Code: #160140
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CAS Number 87885-43-6

science Other reagents with same CAS 87885-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.53 g/mol
Formula C₄H₂ClN₃O₂
thermostat Physical Properties
Boiling Point 283.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its reactive chlorine and electron-withdrawing nitro group allow for selective nucleophilic substitution, enabling the introduction of various functional groups in heterocyclic compounds. Commonly employed in the preparation of dyes and fluorescent probes due to its ability to form stable conjugated systems. Also utilized in research for developing new pyrazine-based bioactive molecules with potential antimicrobial and anticancer properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿930.00
100mg
10-20 days ฿1,760.00
250mg
10-20 days ฿3,130.00
2-Chloro-3-nitropyrazine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its reactive chlorine and electron-withdrawing nitro group allow for selective nucleophilic substitution, enabling the introduction of various functional groups in heterocyclic compounds. Commonly employed in the preparation of dyes and fluorescent probes due to its ability to form stable conjugated systems. Also utilized in research for developing new pyrazine-base

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its reactive chlorine and electron-withdrawing nitro group allow for selective nucleophilic substitution, enabling the introduction of various functional groups in heterocyclic compounds. Commonly employed in the preparation of dyes and fluorescent probes due to its ability to form stable conjugated systems. Also utilized in research for developing new pyrazine-based bioactive molecules with potential antimicrobial and anticancer properties.

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