2-Propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester
[CAS# 65983-31-5]

Identification

• Classification: Organic raw materials >> Carboxylic compounds and derivatives >> Carboxylic esters and their derivatives
• Name: 2-Propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester
• Synonyms: 2-(8-tricyclo[5.2.1.02,6]dec-3-enyloxy)ethyl prop-2-enoate
• Molecular Formula: C₁₅H₂₀O₃
• Molecular Weight: 248.32
• CAS Registry Number: 65983-31-5
• EC Number: 265-991-6
• SMILES: C=CC(=O)OCCOC1CC2CC1C3C2C=CC3

Properties

• Solubility: Practically insoluble (0.042 g/L) (25 ºC), Calc.^*
• Density: 1.12±0.1 g/cm³ (20 ºC 760 Torr), Calc.^*
• Index of Refraction: 1.533, Calc.^*
• Boiling Point: 344.4±42.0 ºC (760 mmHg), Calc.^*
• Flash Point: 142.9±22.5 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07;GHS09 Warning
• Hazard Statements: H315-H319-H335-H411
• Precautionary Statements: P261-P264-P264+P265-P271-P273-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin irritation	Skin Irrit.	2	H315
Eye irritation	Eye Irrit.	2	H319
Specific target organ toxicity - single exposure	STOT SE	3	H335
Chronic hazardous to the aquatic environment	Aquatic Chronic	2	H411

Discovory and Applicatios

2-Propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester, commonly referred to as a complex ester with unique structural characteristics, represents an intriguing compound within the realm of polymer chemistry and materials science. The discovery and development of this chemical substance offer notable advancements in various applications due to its distinctive properties and functionalities.

The compound was first synthesized in the context of expanding the range of functional monomers used in polymer chemistry. Researchers aimed to develop esters with specific reactive sites to improve the mechanical, thermal, and chemical properties of polymeric materials. The synthesis of 2-propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester involved the esterification of 2-propenoic acid with a bicyclic alcohol derivative, resulting in a molecule with both vinyl and ester functional groups. This structure was designed to enhance the reactivity and compatibility of the monomer with other components in polymer formulations.

One of the primary applications of this compound is in the field of UV-curable coatings. Its ability to participate in radical polymerization under UV light allows it to form crosslinked networks that exhibit improved mechanical strength, chemical resistance, and durability. This makes it suitable for high-performance coatings used in automotive finishes, industrial protective coatings, and decorative applications. The compound's unique bicyclic structure contributes to the formation of robust and resilient coatings that can withstand harsh environmental conditions.

In addition to coatings, 2-propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester is employed in the development of adhesives. The ester's reactive groups facilitate strong bonding with various substrates, including metals, plastics, and glass. This capability is crucial for creating durable and high-strength adhesive formulations used in construction, automotive assembly, and electronic device manufacturing. The compound's performance in adhesives is attributed to its ability to form crosslinked networks that enhance adhesion and resistance to environmental factors.

The substance also finds application in the production of specialty resins and composites. Its structural features contribute to the development of materials with specific properties such as high thermal stability, resistance to chemical attack, and enhanced mechanical strength. These characteristics make the compound valuable in industries where advanced materials are required, such as aerospace, marine, and industrial machinery.

Moreover, research into the use of 2-propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester has explored its potential in biomedical applications. Its biocompatibility and functional properties are being investigated for use in medical devices, dental materials, and tissue engineering. The compound's ability to form stable, crosslinked networks makes it a candidate for developing materials with enhanced performance in medical applications.

In summary, 2-propenoic acid 2-[(3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-yl)oxy]ethyl ester is a versatile chemical compound with significant applications in coatings, adhesives, specialty resins, and potentially biomedical materials. Its unique structure and reactivity have led to advancements in polymer science and materials engineering, providing valuable solutions across various industries.