2-Amino-3-benzyloxypyrazine

95%

Reagent Code: #135760
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CAS Number 110223-15-9

science Other reagents with same CAS 110223-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.23 g/mol
Formula C₁₁H₁₁N₃O
badge Registry Numbers
MDL Number MFCD09838954
thermostat Physical Properties
Boiling Point 366°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the creation of nitrogen-containing heterocyclic drugs. Shows potential in the development of central nervous system agents due to its structural affinity with neurotransmitter analogs. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Its benzyloxy and amino functional groups allow for easy modification in combinatorial chemistry, making it valuable in high-throughput screening libraries for drug discovery.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿740.00
inventory 250mg
10-20 days ฿2,270.00

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2-Amino-3-benzyloxypyrazine
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Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the creation of nitrogen-containing heterocyclic drugs. Shows potential in the development of central nervous system agents due to its structural affinity with neurotransmitter analogs. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Its benzyloxy and amino functional groups allow for easy modification in combinatorial chemistry, making it valuable in high-
Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the creation of nitrogen-containing heterocyclic drugs. Shows potential in the development of central nervous system agents due to its structural affinity with neurotransmitter analogs. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Its benzyloxy and amino functional groups allow for easy modification in combinatorial chemistry, making it valuable in high-throughput screening libraries for drug discovery.
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