Tert-Butyl(3-Aminopyridin-2-Yl)Carbamate

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Reagent Code: #84427
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CAS Number 108655-56-7

science Other reagents with same CAS 108655-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.25 g/mol
Formula C₁₀H₁₅N₃O₂
badge Registry Numbers
MDL Number MFCD12028729
thermostat Physical Properties
Boiling Point 313.8±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.202±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

Used in the synthesis of pharmaceutical compounds, particularly as an intermediate in the production of drugs targeting central nervous system disorders. It plays a role in the development of inhibitors for enzymes like kinases, which are crucial in treating cancers and inflammatory diseases. Additionally, it is utilized in organic chemistry research for constructing complex molecules due to its protective group properties for amines, facilitating selective reactions. Its application extends to the preparation of bioactive molecules in medicinal chemistry, aiding in the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,680.00
inventory 250mg
10-20 days ฿8,190.00
inventory 1g
10-20 days ฿16,380.00
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Tert-Butyl(3-Aminopyridin-2-Yl)Carbamate
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Used in the synthesis of pharmaceutical compounds, particularly as an intermediate in the production of drugs targeting central nervous system disorders. It plays a role in the development of inhibitors for enzymes like kinases, which are crucial in treating cancers and inflammatory diseases. Additionally, it is utilized in organic chemistry research for constructing complex molecules due to its protective group properties for amines, facilitating selective reactions. Its application extends to the prepa

Used in the synthesis of pharmaceutical compounds, particularly as an intermediate in the production of drugs targeting central nervous system disorders. It plays a role in the development of inhibitors for enzymes like kinases, which are crucial in treating cancers and inflammatory diseases. Additionally, it is utilized in organic chemistry research for constructing complex molecules due to its protective group properties for amines, facilitating selective reactions. Its application extends to the preparation of bioactive molecules in medicinal chemistry, aiding in the discovery of new therapeutic agents.

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