6-Methoxy-2-(4-methoxyphenyl) benzo[b]thiophene

98%

Reagent Code: #205266
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CAS Number 63675-74-1

science Other reagents with same CAS 63675-74-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.35 g/mol
Formula C₁₆H₁₄O₂S
badge Registry Numbers
EC Number 264-408-2
MDL Number MFCD02083138
thermostat Physical Properties
Melting Point 191-197 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of selective estrogen receptor modulators (SERMs). It serves as a key building block in creating compounds with potential therapeutic effects for hormone-related conditions such as osteoporosis and breast cancer. Its structural features allow for high binding affinity to estrogen receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent probes due to its favorable photophysical properties, useful in biochemical imaging and assay technologies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿168.00
5g
10-20 days ฿550.00
25g
10-20 days ฿1,960.00
100g
10-20 days ฿6,900.00
6-Methoxy-2-(4-methoxyphenyl) benzo[b]thiophene
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of selective estrogen receptor modulators (SERMs). It serves as a key building block in creating compounds with potential therapeutic effects for hormone-related conditions such as osteoporosis and breast cancer. Its structural features allow for high binding affinity to estrogen receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent probes due to its favorable ph

Used in the synthesis of pharmaceutical intermediates, particularly in the development of selective estrogen receptor modulators (SERMs). It serves as a key building block in creating compounds with potential therapeutic effects for hormone-related conditions such as osteoporosis and breast cancer. Its structural features allow for high binding affinity to estrogen receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent probes due to its favorable photophysical properties, useful in biochemical imaging and assay technologies.

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