Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate

≥95%

Reagent Code: #183618
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CAS Number 82962-54-7

science Other reagents with same CAS 82962-54-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.22 g/mol
Formula C₉H₁₆O₄
badge Registry Numbers
MDL Number MFCD11975772
thermostat Physical Properties
Boiling Point 217.5±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its cyclic acetal structure provides stability and selectivity in multi-step reactions, making it valuable for protecting carbonyl groups during synthesis. Commonly employed in the development of active ingredients in crop protection products and in the construction of complex molecules requiring stereochemical control. Also utilized in fragrance and flavor synthesis due to its ability to act as a masked aldehyde equivalent.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,600.00
inventory 10g
10-20 days ฿2,680.00
inventory 25g
10-20 days ฿5,570.00
inventory 100g
10-20 days ฿21,880.00

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Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its cyclic acetal structure provides stability and selectivity in multi-step reactions, making it valuable for protecting carbonyl groups during synthesis. Commonly employed in the development of active ingredients in crop protection products and in the construction of complex molecules requiring stereochemical control. Also utilized in fragrance and flavor synthesis due to its ability to a

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its cyclic acetal structure provides stability and selectivity in multi-step reactions, making it valuable for protecting carbonyl groups during synthesis. Commonly employed in the development of active ingredients in crop protection products and in the construction of complex molecules requiring stereochemical control. Also utilized in fragrance and flavor synthesis due to its ability to act as a masked aldehyde equivalent.

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