N-(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropionamide

95%

Reagent Code: #72745
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CAS Number 149765-15-1

science Other reagents with same CAS 149765-15-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.7 g/mol
Formula C₁₁H₁₃ClN₄O
badge Registry Numbers
MDL Number MFCD11109809
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial in targeted cancer therapies. The compound’s pyrrolo[2,3-d]pyrimidine core is a common scaffold in drugs designed to modulate protein kinases, making it a significant building block in the creation of potential anticancer agents. Additionally, its application extends to research focused on autoimmune diseases and inflammatory conditions, where kinase inhibition plays a therapeutic role. Its specific functional groups allow for further chemical modifications, enabling the exploration of structure-activity relationships in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,538.00
inventory 25mg
10-20 days ฿729.00

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N-(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropionamide
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial in targeted cancer therapies. The compound’s pyrrolo[2,3-d]pyrimidine core is a common scaffold in drugs designed to modulate protein kinases, making it a significant building block in the creation of potential anticancer agents. Additionally, its application extends to research focused on autoimmune diseases and inflammatory conditions, where kinase inhibition plays a therapeutic role. Its specific functional groups allow for further chemical modifications, enabling the exploration of structure-activity relationships in drug discovery programs.
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