(E)-Oct-4-ene-1,8-dioic Acid

95%

Reagent Code: #184159
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CAS Number 48059-97-8

science Other reagents with same CAS 48059-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₈H₁₂O₄
thermostat Physical Properties
Melting Point 175-176 °C(lit.)
Boiling Point 373.11 ºC at 760 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.2 g/cm3 at 25 °C (lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of cyclic compounds through ring-closing metathesis reactions. Its structure featuring a central double bond with terminal carboxylic acid groups allows for selective functionalization, making it valuable in pharmaceutical and polymer chemistry. It serves in the synthesis of specialty monomers for biodegradable polyesters and in the development of bioactive molecules due to its ability to mimic natural fatty acid metabolites. Also employed in cross-coupling reactions to build complex molecular architectures in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,090.00
inventory 5g
10-20 days ฿4,150.00
inventory 10g
10-20 days ฿7,490.00
inventory 50g
10-20 days ฿27,540.00
inventory 100g
10-20 days ฿54,000.00
inventory 25g
10-20 days ฿13,220.00

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(E)-Oct-4-ene-1,8-dioic Acid
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Used as a key intermediate in organic synthesis, particularly in the preparation of cyclic compounds through ring-closing metathesis reactions. Its structure featuring a central double bond with terminal carboxylic acid groups allows for selective functionalization, making it valuable in pharmaceutical and polymer chemistry. It serves in the synthesis of specialty monomers for biodegradable polyesters and in the development of bioactive molecules due to its ability to mimic natural fatty acid metabolites

Used as a key intermediate in organic synthesis, particularly in the preparation of cyclic compounds through ring-closing metathesis reactions. Its structure featuring a central double bond with terminal carboxylic acid groups allows for selective functionalization, making it valuable in pharmaceutical and polymer chemistry. It serves in the synthesis of specialty monomers for biodegradable polyesters and in the development of bioactive molecules due to its ability to mimic natural fatty acid metabolites. Also employed in cross-coupling reactions to build complex molecular architectures in medicinal chemistry research.

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