(Trimethylsilyl)acetic acid

98%

Reagent Code: #239913
label
Alias (Trimethylsilyl)acetic acid
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CAS Number 2345-38-2

science Other reagents with same CAS 2345-38-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.23 g/mol
Formula C₅H₁₂O₂Si
badge Registry Numbers
EC Number 219-067-4
MDL Number MFCD00042651
thermostat Physical Properties
Melting Point 39-42 °C(lit.)
Boiling Point 90-95°C 10mm
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

(Trimethylsilyl)acetic acid is an organosilicon compound utilized in organic synthesis as a building block for introducing the (trimethylsilyl)methyl (TMS-CH2−) functionality. It is particularly valuable in Peterson olefination reactions, where its anion adds to carbonyl compounds to form β-hydroxysilanes that eliminate to yield alkenes, enabling stereoselective alkene synthesis from aldehydes and ketones. The compound also serves as a precursor for generating stabilized carbanions in aldol-type additions and in the preparation of α-silyl esters or acids. Due to the labile silyl group, it facilitates deprotection strategies in multi-step syntheses. Commonly applied in pharmaceutical and agrochemical research for creating complex intermediates with high purity and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,860.00
(Trimethylsilyl)acetic acid
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(Trimethylsilyl)acetic acid is an organosilicon compound utilized in organic synthesis as a building block for introducing the (trimethylsilyl)methyl (TMS-CH2−) functionality. It is particularly valuable in Peterson olefination reactions, where its anion adds to carbonyl compounds to form β-hydroxysilanes that eliminate to yield alkenes, enabling stereoselective alkene synthesis from aldehydes and ketones. The compound also serves as a precursor for generating stabilized carbanions in aldol-type
(Trimethylsilyl)acetic acid is an organosilicon compound utilized in organic synthesis as a building block for introducing the (trimethylsilyl)methyl (TMS-CH2−) functionality. It is particularly valuable in Peterson olefination reactions, where its anion adds to carbonyl compounds to form β-hydroxysilanes that eliminate to yield alkenes, enabling stereoselective alkene synthesis from aldehydes and ketones. The compound also serves as a precursor for generating stabilized carbanions in aldol-type additions and in the preparation of α-silyl esters or acids. Due to the labile silyl group, it facilitates deprotection strategies in multi-step syntheses. Commonly applied in pharmaceutical and agrochemical research for creating complex intermediates with high purity and selectivity.
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