2-Chloro-3-(methoxymethyl)pyrazine

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Reagent Code: #160011
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CAS Number 1289387-97-8

science Other reagents with same CAS 1289387-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.59 g/mol
Formula C₆H₇ClN₂O
thermostat Physical Properties
Boiling Point 198.3±35.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for antiviral and antibacterial agents. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocyclic compounds. It is also employed in agrochemical synthesis, contributing to the creation of certain pesticides and herbicides due to its reactivity and stability in multi-step reactions. Additionally, it serves in research laboratories for the preparation of pyrazine-based derivatives with potential biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿55,290.00
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2-Chloro-3-(methoxymethyl)pyrazine
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for antiviral and antibacterial agents. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocyclic compounds. It is also employed in agrochemical synthesis, contributing to the creation of certain pesticides and herbicides due to its reactivity and stability in multi-step reactions. Additionally

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for antiviral and antibacterial agents. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocyclic compounds. It is also employed in agrochemical synthesis, contributing to the creation of certain pesticides and herbicides due to its reactivity and stability in multi-step reactions. Additionally, it serves in research laboratories for the preparation of pyrazine-based derivatives with potential biological activity.

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