7-(Tert-butyl)-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-ol

97%

Reagent Code: #244851
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CAS Number 380902-66-9

science Other reagents with same CAS 380902-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.37 g/mol
Formula C₁₄H₁₈N₂OS
badge Registry Numbers
MDL Number MFCD02995063
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports selective binding to enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design drugs targeting inflammatory diseases and certain solid tumors. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid, fused-ring framework that enhances metabolic stability and bioavailability in lead compounds.

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inventory 1g
10-20 days ฿13,680.00

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7-(Tert-butyl)-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-ol
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports selective binding to enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design drugs targeting inflammatory diseases and certain solid tumors. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid, fused-ring framework that enhances metabolic stabili

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports selective binding to enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design drugs targeting inflammatory diseases and certain solid tumors. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid, fused-ring framework that enhances metabolic stability and bioavailability in lead compounds.

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