tert-Butyl 5h-spiro[pyrido[3,2-e]pyrrolo[1,2-a]pyrazine-6,3'-pyrrolidine]-1'-carboxylate

95%

Reagent Code: #156045
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CAS Number 1290625-92-1

science Other reagents with same CAS 1290625-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.40 g/mol
Formula C₁₈H₂₂N₄O₂
badge Registry Numbers
MDL Number MFCD19442501
thermostat Physical Properties
Boiling Point 514.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors for cancer treatment. Its spirocyclic structure provides structural rigidity and selectivity, enhancing drug potency and metabolic stability. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems found in bioactive molecules. Also utilized in research settings to explore new central nervous system agents due to its ability to cross the blood-brain barrier.

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inventory 1g
10-20 days ฿100,140.00

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tert-Butyl 5h-spiro[pyrido[3,2-e]pyrrolo[1,2-a]pyrazine-6,3'-pyrrolidine]-1'-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors for cancer treatment. Its spirocyclic structure provides structural rigidity and selectivity, enhancing drug potency and metabolic stability. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems found in bioactive molecules. Also utilized in research settings to explore new central nervous system agents due to its ability to cross the blood-brain barrier.

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors for cancer treatment. Its spirocyclic structure provides structural rigidity and selectivity, enhancing drug potency and metabolic stability. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems found in bioactive molecules. Also utilized in research settings to explore new central nervous system agents due to its ability to cross the blood-brain barrier.

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