Tert-Butyl 4-(5-amino-1H-1,2,4-triazol-3-yl)piperazine-1-carboxylate

90%

Reagent Code: #238206
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CAS Number 1263286-45-8

science Other reagents with same CAS 1263286-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.321 g/mol
Formula C₁₁H₂₀N₆O₂
thermostat Physical Properties
Boiling Point 583.0±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure supports the construction of compounds with potential anticonvulsant, antidepressant, or antipsychotic activity. The protected amine and triazole functionalities allow for selective modifications in multi-step synthetic routes, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,900.00
Tert-Butyl 4-(5-amino-1H-1,2,4-triazol-3-yl)piperazine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure supports the construction of compounds with potential anticonvulsant, antidepressant, or antipsychotic activity. The protected amine and triazole functionalities allow for selective modifications in multi-step synthetic routes, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability.<

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure supports the construction of compounds with potential anticonvulsant, antidepressant, or antipsychotic activity. The protected amine and triazole functionalities allow for selective modifications in multi-step synthetic routes, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability.

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