Chlorotriethylsilane

98%

Reagent Code: #88282
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Alias Triethylchlorosilane
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CAS Number 994-30-9

science Other reagents with same CAS 994-30-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.72 g/mol
Formula C₆H₁₅ClSi
badge Registry Numbers
EC Number 213-615-6
MDL Number MFCD00000507
thermostat Physical Properties
Melting Point -50°C
Boiling Point 142-144 °C(lit.)
inventory_2 Storage & Handling
Density 0.898 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

Used primarily as a reagent in organic synthesis for the introduction of the triethylsilyl group, which serves as a protective group for alcohols and other sensitive functional groups. It is particularly valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where selective protection and deprotection of hydroxyl groups are required. Additionally, it finds application in the modification of surfaces and materials, where its reactivity with hydroxyl groups on surfaces like glass or silica is exploited to impart hydrophobic properties. This makes it useful in the production of water-repellent coatings and in the preparation of chromatographic stationary phases.

format_list_bulleted Product Specification

Test Parameter Specification
Refractive Index (n20D) 1.43-1.432
Purity 98-100
Specific Gravity (20°C) 0.897-0.903
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms to structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿320.00
inventory 25ml
10-20 days ฿610.00
inventory 100ml
10-20 days ฿1,560.00
inventory 500ml
10-20 days ฿7,520.00

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Chlorotriethylsilane
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Used primarily as a reagent in organic synthesis for the introduction of the triethylsilyl group, which serves as a protective group for alcohols and other sensitive functional groups. It is particularly valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where selective protection and deprotection of hydroxyl groups are required. Additionally, it finds application in the modification of surfaces and materials, where its reactivity with hydroxyl groups

Used primarily as a reagent in organic synthesis for the introduction of the triethylsilyl group, which serves as a protective group for alcohols and other sensitive functional groups. It is particularly valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where selective protection and deprotection of hydroxyl groups are required. Additionally, it finds application in the modification of surfaces and materials, where its reactivity with hydroxyl groups on surfaces like glass or silica is exploited to impart hydrophobic properties. This makes it useful in the production of water-repellent coatings and in the preparation of chromatographic stationary phases.

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