2-(4-Hydroxyphenyl)benzo[b]thiophene-6-ol

≥98%(GC)

Reagent Code: #85102
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CAS Number 63676-22-2

science Other reagents with same CAS 63676-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.29 g/mol
Formula C₁₄H₁₀O₂S
badge Registry Numbers
MDL Number MFCD16619490
thermostat Physical Properties
Melting Point 295°C(分解)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound serves as a key intermediate in the synthesis of selective estrogen receptor modulators (SERMs), such as raloxifene, for pharmaceutical applications in treating hormone-related diseases like breast cancer. Its structure mimics estrogen, enabling it to bind to estrogen receptors and inhibit cancer cell growth. Additionally, owing to its extended π-conjugated system and fluorescence properties, it is utilized in the development of organic light-emitting diodes (OLEDs) as a component in emissive layers to improve efficiency and brightness. It also contributes to advanced optoelectronic devices, sensors for biological molecule detection, and research in photoresponsive materials and photodynamic therapy.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,745.00
inventory 250mg
10-20 days ฿12,366.00

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2-(4-Hydroxyphenyl)benzo[b]thiophene-6-ol
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This compound serves as a key intermediate in the synthesis of selective estrogen receptor modulators (SERMs), such as raloxifene, for pharmaceutical applications in treating hormone-related diseases like breast cancer. Its structure mimics estrogen, enabling it to bind to estrogen receptors and inhibit cancer cell growth. Additionally, owing to its extended π-conjugated system and fluorescence properties, it is utilized in the development of organic light-emitting diodes (OLEDs) as a component in emissi

This compound serves as a key intermediate in the synthesis of selective estrogen receptor modulators (SERMs), such as raloxifene, for pharmaceutical applications in treating hormone-related diseases like breast cancer. Its structure mimics estrogen, enabling it to bind to estrogen receptors and inhibit cancer cell growth. Additionally, owing to its extended π-conjugated system and fluorescence properties, it is utilized in the development of organic light-emitting diodes (OLEDs) as a component in emissive layers to improve efficiency and brightness. It also contributes to advanced optoelectronic devices, sensors for biological molecule detection, and research in photoresponsive materials and photodynamic therapy.

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