Phenol, 2-[4-bromo-1-[5-(1,1-dimethylethyl)[1,1∏-biphenyl]-2-yl]-1H-benzimidazol-2-yl]-4,6-bis(1,1-dimethylethyl)- (ACI)

98%

Reagent Code: #223293
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CAS Number 2361613-60-5

science Other reagents with same CAS 2361613-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 609.6382 g/mol
Formula C₃₇H₄₁BrN₂O
thermostat Physical Properties
Boiling Point 686.3±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of selective estrogen receptor modulators (SERMs), particularly in the development of pharmaceuticals for hormone-dependent conditions such as breast cancer. Its structural features enable high affinity binding to estrogen receptors, making it valuable in drug research and development. The compound is also employed in the preparation of potent antiestrogenic agents used in both therapeutic and diagnostic applications. Due to its stability and specific reactivity, it serves as a building block in medicinal chemistry for optimizing receptor selectivity and pharmacokinetic properties in new drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,000.00
inventory 250mg
10-20 days ฿12,800.00
inventory 1g
10-20 days ฿19,200.00
inventory 5g
10-20 days ฿64,000.00

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Phenol, 2-[4-bromo-1-[5-(1,1-dimethylethyl)[1,1∏-biphenyl]-2-yl]-1H-benzimidazol-2-yl]-4,6-bis(1,1-dimethylethyl)- (ACI)
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Used primarily as a key intermediate in the synthesis of selective estrogen receptor modulators (SERMs), particularly in the development of pharmaceuticals for hormone-dependent conditions such as breast cancer. Its structural features enable high affinity binding to estrogen receptors, making it valuable in drug research and development. The compound is also employed in the preparation of potent antiestrogenic agents used in both therapeutic and diagnostic applications. Due to its stability and specific

Used primarily as a key intermediate in the synthesis of selective estrogen receptor modulators (SERMs), particularly in the development of pharmaceuticals for hormone-dependent conditions such as breast cancer. Its structural features enable high affinity binding to estrogen receptors, making it valuable in drug research and development. The compound is also employed in the preparation of potent antiestrogenic agents used in both therapeutic and diagnostic applications. Due to its stability and specific reactivity, it serves as a building block in medicinal chemistry for optimizing receptor selectivity and pharmacokinetic properties in new drug candidates.

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