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.

Available Sizes & Pricing

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