73597-26-9

Basic information

• Product Name: 2-[({[(1R,5R)-5-isocyanato-1,3,3-trimethylcyclohexyl]methyl}carbamoyl)oxy]ethyl 2-methylprop-2-enoate
• CAS NO: 73597-26-9
• Molecular Formula: C₁₈H₂₈N₂O₅
• Molecular Weight: 352.4253
• Mol File: 73597-26-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 460.4°C at 760 mmHg
• Flash Point: 232.2°C
• Density: 1.12g/cm³
• Vapor Pressure: 1.17E-08mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: 2-[({[(1R,5R)-5-isocyanato-1,3,3-trimethylcyclohexyl]methyl}carbamoyl)oxy]ethyl 2-methylprop-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[({[(1R,5R)-5-isocyanato-1,3,3-trimethylcyclohexyl]methyl}carbamoyl)oxy]ethyl 2-methylprop-2-enoate(73597-26-9)
• EPA Substance Registry System: 2-[({[(1R,5R)-5-isocyanato-1,3,3-trimethylcyclohexyl]methyl}carbamoyl)oxy]ethyl 2-methylprop-2-enoate(73597-26-9)

Safety Data

• Hazardous Substances Data: 73597-26-9(Hazardous Substances Data)

Usage

Molecular structure

The compound has a complex molecular structure with a combination of various functional groups, including an isocyanate group, a carbamoyl group, and an ester group.

Isocyanate group

The presence of the isocyanate group (-NCO) makes the compound useful in the production of polyurethane foams, adhesives, and coatings.

Carbamoyl group

The carbamoyl group (-NHCOO-) in the compound gives it potential use as a crosslinking agent, which can help improve the strength and durability of materials.

Ester group

The ester group (-COO-) in the compound contributes to its potential use as a component in the formulation of various materials, such as polymers and plastics.

Versatility

The specific chemical structure and functional groups of the compound make it a valuable and versatile compound for use in a wide range of industrial and scientific applications.

Building block

The compound serves as a building block for the synthesis of other chemical compounds, making it an important intermediate in various chemical reactions.

Industrial applications

Due to its unique properties and functional groups, the compound is utilized in various industrial applications, including the production of foams, adhesives, coatings, and other materials.

Upstream product

• 868-77-9 2-methyl-2-propenoic acid 2-hydroxyethyl ester 
• 4098-71-9 isophorone diisocyanate 

Downstream Products

• 1160296-68-3 C₂₈H₄₁N₃O₉ 
• 1308247-91-7 C₁₈H₃₁N₃O₆ 

Relevant articles and documents

A multi-functional polyurethane acrylate and its preparation method and application

The invention discloses multifunctional urethane acrylate as well as a preparation method and an application thereof. The preparation method comprises the steps: under the protection of nitrogen, dropwise adding acrylic acid hydroxy ester or methacrylic a

Variable-temperature time-resolved emission spectra studies of random pyrene urethane methacrylate copolymers with high pyrene incorporation

A series of random co-polyurethane methacrylate comb polymers with pyrene (Py) and 3-pentadecylphenol (PDP) as pendant units were prepared by free radical polymerization. The pyrene labeling was varied from 1 to 100 mol %. The excimer emission of these copolymers were studied as a function of both time and temperature using time-resolved emission spectra (TRES) experiments and variable-temperature steady-state fluorescence measurements. Variable-temperature steady-state as well as decay experiments showed that the contribution from excimers via diffusional encounters increased at the cost of pyrene monomer as the temperature increased until a??50 C; beyond which nonradiative losses predominated. TRES collected at 25 and 70 C were compared to study the nature and origin of emitting species as a function of pyrene loading. TRES at 25 C clearly indicated the presence of ground-state pyrene dimers with emission centered at a??435 nm which soon gave way to emission centered around 465 and 485 nm in the time-gated spectra collected at higher time intervals. In TRES collected at 70 C, excimer emission centered at 465 and 485 nm was very high even at short time scales. The lowest pyrene loaded polymer PIHPDP-1Py did not exhibit excimer emission in the TRES collected at 25 C as well as 70 C. ? 2013 American Chemical Society.

HIGH ADHESIVE ACRYLATE MONOMER AND METHOD FOR PREPARING THE SAME

A high adhesive acrylate monomer has a specific chemistry figure. This monomer may be easily prepared in a simplified way, and various linkers may be used between L-DOPA and an acrylate group attached to a tail of L-DOPA, so molecular weight and size of the entire material may be easily controlled. Also, various kinds of acrylate to be combined to a isocyanate compound used as a linker may be selected, so various molecules may be easily composed.