1,3-Bis(4-methoxyphenyl)-1,1,3,3-tetramethyldisiloxane

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Reagent Code: #156107
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CAS Number 122571-17-9

science Other reagents with same CAS 122571-17-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.57 g/mol
Formula C₁₈H₂₆O₃Si₂
badge Registry Numbers
MDL Number MFCD09266156
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a silicone-based intermediate in the synthesis of advanced organic materials, particularly in the development of liquid crystal compounds and OLED (organic light-emitting diode) materials. Its structure provides thermal stability and solubility, making it suitable for use in electronic-grade chemicals. Also employed in surface treatment agents to modify surface energy and improve adhesion in specialty coatings. Additionally, it acts as a protecting group reagent in complex organic syntheses due to the stability and selective reactivity of the disiloxane backbone.

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inventory 1g
10-20 days ฿7,590.00
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1,3-Bis(4-methoxyphenyl)-1,1,3,3-tetramethyldisiloxane
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Used as a silicone-based intermediate in the synthesis of advanced organic materials, particularly in the development of liquid crystal compounds and OLED (organic light-emitting diode) materials. Its structure provides thermal stability and solubility, making it suitable for use in electronic-grade chemicals. Also employed in surface treatment agents to modify surface energy and improve adhesion in specialty coatings. Additionally, it acts as a protecting group reagent in complex organic syntheses due t

Used as a silicone-based intermediate in the synthesis of advanced organic materials, particularly in the development of liquid crystal compounds and OLED (organic light-emitting diode) materials. Its structure provides thermal stability and solubility, making it suitable for use in electronic-grade chemicals. Also employed in surface treatment agents to modify surface energy and improve adhesion in specialty coatings. Additionally, it acts as a protecting group reagent in complex organic syntheses due to the stability and selective reactivity of the disiloxane backbone.

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