Magnesium (Z)-3-(2,4-dimethoxyphenyl)but-2-enoate

98%

Reagent Code: #204119
fingerprint
CAS Number 54283-65-7

science Other reagents with same CAS 54283-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.76 g/mol
Formula C₂₄H₂₆MgO₈
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of flavonoid derivatives and other bioactive molecules. Its structure supports carbon-carbon bond formation in reactions such as aldol condensations and Michael additions. Commonly employed in pharmaceutical research for constructing complex natural product frameworks. Also utilized in asymmetric synthesis due to its ability to form chiral centers under catalytic conditions. Shows utility in the development of light-sensitive compounds and in materials science for designing functional organic materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿15,200.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Magnesium (Z)-3-(2,4-dimethoxyphenyl)but-2-enoate
No image available

Used as a key intermediate in organic synthesis, particularly in the preparation of flavonoid derivatives and other bioactive molecules. Its structure supports carbon-carbon bond formation in reactions such as aldol condensations and Michael additions. Commonly employed in pharmaceutical research for constructing complex natural product frameworks. Also utilized in asymmetric synthesis due to its ability to form chiral centers under catalytic conditions. Shows utility in the development of light-sensitiv

Used as a key intermediate in organic synthesis, particularly in the preparation of flavonoid derivatives and other bioactive molecules. Its structure supports carbon-carbon bond formation in reactions such as aldol condensations and Michael additions. Commonly employed in pharmaceutical research for constructing complex natural product frameworks. Also utilized in asymmetric synthesis due to its ability to form chiral centers under catalytic conditions. Shows utility in the development of light-sensitive compounds and in materials science for designing functional organic materials.

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...