1,5-Dioxaspiro[5.5]undecane,3,3-dimethyl-

≥95%

Reagent Code: #167841
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CAS Number 707-29-9

science Other reagents with same CAS 707-29-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.2753 g/mol
Formula C₁₁H₂₀O₂
badge Registry Numbers
MDL Number MFCD00126982
thermostat Physical Properties
Boiling Point 110.0-110.5 °C at 19-20 mmHg
inventory_2 Storage & Handling
Density 0.98±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a protecting group reagent in organic synthesis, particularly for diols. Its primary application is in the formation of spiro acetals, which stabilize sensitive functional groups during multi-step syntheses. Commonly employed in pharmaceutical and fragrance chemistry due to its ability to mask and later release diol structures under mild acidic conditions. Also utilized in polymer chemistry as a building block for specialty monomers, contributing to the development of hydrolytically stable materials.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿19,200.00
inventory 100mg
10-20 days ฿32,000.00
inventory 250mg
10-20 days ฿57,600.00

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1,5-Dioxaspiro[5.5]undecane,3,3-dimethyl-
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Used as a protecting group reagent in organic synthesis, particularly for diols. Its primary application is in the formation of spiro acetals, which stabilize sensitive functional groups during multi-step syntheses. Commonly employed in pharmaceutical and fragrance chemistry due to its ability to mask and later release diol structures under mild acidic conditions. Also utilized in polymer chemistry as a building block for specialty monomers, contributing to the development of hydrolytically stable materi

Used as a protecting group reagent in organic synthesis, particularly for diols. Its primary application is in the formation of spiro acetals, which stabilize sensitive functional groups during multi-step syntheses. Commonly employed in pharmaceutical and fragrance chemistry due to its ability to mask and later release diol structures under mild acidic conditions. Also utilized in polymer chemistry as a building block for specialty monomers, contributing to the development of hydrolytically stable materials.

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