4-(Trimethylsilyl)benzoic acid

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Reagent Code: #242744
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CAS Number 15290-29-6

science Other reagents with same CAS 15290-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.30 g/mol
Formula C₁₀H₁₄O₂Si
badge Registry Numbers
MDL Number MFCD00092492
thermostat Physical Properties
Melting Point 116.5-117.5 °C
Boiling Point 281.4±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.04±0.1 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

4-(Trimethylsilyl)benzoic acid serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The trimethylsilyl group on the aromatic ring functions as a directing or activating substituent, enhancing reactivity and selectivity in various organic transformations, including cross-coupling reactions such as Hiyama-Denmark coupling for efficient carbon-carbon bond formation. It is also utilized in the preparation of silyl-modified building blocks for peptide and nucleotide analogs, where the carboxylic acid group can be further functionalized. The lipophilic trimethylsilyl moiety improves solubility in non-aqueous media, facilitating applications in chromatography as a reference standard and in material science for developing heat- or chemically-resistant polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,570.00
inventory 250mg
10-20 days ฿6,010.00
inventory 1g
10-20 days ฿15,740.00

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4-(Trimethylsilyl)benzoic acid
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4-(Trimethylsilyl)benzoic acid serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The trimethylsilyl group on the aromatic ring functions as a directing or activating substituent, enhancing reactivity and selectivity in various organic transformations, including cross-coupling reactions such as Hiyama-Denmark coupling for efficient carbon-carbon bond formation. It is also utilized in the preparation of silyl-modified building blocks for peptide and nucleotide analogs, whe

4-(Trimethylsilyl)benzoic acid serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The trimethylsilyl group on the aromatic ring functions as a directing or activating substituent, enhancing reactivity and selectivity in various organic transformations, including cross-coupling reactions such as Hiyama-Denmark coupling for efficient carbon-carbon bond formation. It is also utilized in the preparation of silyl-modified building blocks for peptide and nucleotide analogs, where the carboxylic acid group can be further functionalized. The lipophilic trimethylsilyl moiety improves solubility in non-aqueous media, facilitating applications in chromatography as a reference standard and in material science for developing heat- or chemically-resistant polymers.

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