4,5-Dimethyl-1,3-dioxolan-2-one

95%

Reagent Code: #179817
fingerprint
CAS Number 4437-70-1

science Other reagents with same CAS 4437-70-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 116.12 g/mol
Formula C₅H₈O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of fine chemicals and pharmaceuticals, particularly in the preparation of chiral auxiliaries and asymmetric synthesis. It serves as a building block for lactone-containing compounds due to its cyclic carbonate structure, which can undergo ring-opening reactions with nucleophiles such as amines, alcohols, and thiols. Commonly applied in the development of biodegradable polymers and as a solvent or additive in lithium-ion battery electrolytes, where it improves thermal stability and enhances electrode performance. Also utilized in the fragrance industry for the controlled release of active ingredients owing to its ability to form stable derivatives.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,540.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4,5-Dimethyl-1,3-dioxolan-2-one
No image available

Used as a key intermediate in the synthesis of fine chemicals and pharmaceuticals, particularly in the preparation of chiral auxiliaries and asymmetric synthesis. It serves as a building block for lactone-containing compounds due to its cyclic carbonate structure, which can undergo ring-opening reactions with nucleophiles such as amines, alcohols, and thiols. Commonly applied in the development of biodegradable polymers and as a solvent or additive in lithium-ion battery electrolytes, where it improves t

Used as a key intermediate in the synthesis of fine chemicals and pharmaceuticals, particularly in the preparation of chiral auxiliaries and asymmetric synthesis. It serves as a building block for lactone-containing compounds due to its cyclic carbonate structure, which can undergo ring-opening reactions with nucleophiles such as amines, alcohols, and thiols. Commonly applied in the development of biodegradable polymers and as a solvent or additive in lithium-ion battery electrolytes, where it improves thermal stability and enhances electrode performance. Also utilized in the fragrance industry for the controlled release of active ingredients owing to its ability to form stable derivatives.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...