tert-Butyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetate

98%

Reagent Code: #36612
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CAS Number 1082827-81-3

science Other reagents with same CAS 1082827-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.27282 g/mol
Formula C₁₁H₁₈N₂O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various heterocyclic compounds. Its structure, featuring a pyrazole ring and an ester functional group, makes it suitable for constructing complex molecules in pharmaceutical research. It is often employed in the development of biologically active compounds, particularly in the synthesis of potential drug candidates targeting inflammation, cancer, or other diseases. Additionally, its ester group allows for further chemical modifications, enabling the creation of derivatives with tailored properties for specific applications in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,681.00
inventory 250mg
10-20 days ฿1,404.00

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tert-Butyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various heterocyclic compounds. Its structure, featuring a pyrazole ring and an ester functional group, makes it suitable for constructing complex molecules in pharmaceutical research. It is often employed in the development of biologically active compounds, particularly in the synthesis of potential drug candidates targeting inflammation, cancer, or other diseases. Additionally, its ester group allow
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various heterocyclic compounds. Its structure, featuring a pyrazole ring and an ester functional group, makes it suitable for constructing complex molecules in pharmaceutical research. It is often employed in the development of biologically active compounds, particularly in the synthesis of potential drug candidates targeting inflammation, cancer, or other diseases. Additionally, its ester group allows for further chemical modifications, enabling the creation of derivatives with tailored properties for specific applications in medicinal chemistry.
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