1,4-Phenylenediacryloyl chloride

97%

Reagent Code: #226683
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CAS Number 35288-49-4

science Other reagents with same CAS 35288-49-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.1 g/mol
Formula C₁₂H₈Cl₂O₂
badge Registry Numbers
MDL Number MFCD01109676
thermostat Physical Properties
Melting Point >300 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a crosslinking agent in polymer chemistry, enabling the formation of rigid, thermally stable networks in specialty resins. Its acyl chloride groups readily react with amines or alcohols, making it valuable in synthesizing polyamides and polyesters with enhanced mechanical strength. It is also employed in the development of functional coatings and thin films where high chemical resistance and structural integrity are required. Additionally, it serves as a building block in the preparation of conjugated polymers for optoelectronic applications due to the aromatic backbone that supports electron delocalization.

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inventory 1g
10-20 days ฿15,800.00

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1,4-Phenylenediacryloyl chloride
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Used primarily as a crosslinking agent in polymer chemistry, enabling the formation of rigid, thermally stable networks in specialty resins. Its acyl chloride groups readily react with amines or alcohols, making it valuable in synthesizing polyamides and polyesters with enhanced mechanical strength. It is also employed in the development of functional coatings and thin films where high chemical resistance and structural integrity are required. Additionally, it serves as a building block in the preparatio

Used primarily as a crosslinking agent in polymer chemistry, enabling the formation of rigid, thermally stable networks in specialty resins. Its acyl chloride groups readily react with amines or alcohols, making it valuable in synthesizing polyamides and polyesters with enhanced mechanical strength. It is also employed in the development of functional coatings and thin films where high chemical resistance and structural integrity are required. Additionally, it serves as a building block in the preparation of conjugated polymers for optoelectronic applications due to the aromatic backbone that supports electron delocalization.

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