1,2,3,4-Tetrahydronaphthalene-1,5-diol

95%

Reagent Code: #242319
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CAS Number 40771-26-4

science Other reagents with same CAS 40771-26-4

blur_circular Chemical Specifications

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Weight 164.2 g/mol
Formula C₁₀H₁₂O₂
badge Registry Numbers
MDL Number MFCD00001735
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of estrogen receptor modulators. It serves as a building block in organic reactions where a rigid, partially saturated aromatic scaffold is required. Its diol functionality allows for selective derivatization, making it useful in medicinal chemistry for creating analogs with improved bioavailability or binding affinity. Also employed in research settings to study polyphenolic compound behavior and antioxidant activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,770.00
inventory 250mg
10-20 days ฿2,940.00
inventory 1g
10-20 days ฿6,160.00

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1,2,3,4-Tetrahydronaphthalene-1,5-diol
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of estrogen receptor modulators. It serves as a building block in organic reactions where a rigid, partially saturated aromatic scaffold is required. Its diol functionality allows for selective derivatization, making it useful in medicinal chemistry for creating analogs with improved bioavailability or binding affinity. Also employed in research settings to study polyphenolic compound behavior and antiox

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of estrogen receptor modulators. It serves as a building block in organic reactions where a rigid, partially saturated aromatic scaffold is required. Its diol functionality allows for selective derivatization, making it useful in medicinal chemistry for creating analogs with improved bioavailability or binding affinity. Also employed in research settings to study polyphenolic compound behavior and antioxidant activity.

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