178889-47-9

Basic information

• Product Name: 1-METHYLCYCLOHEXYL ACRYLATE
• Synonyms: 1-METHYLCYCLOHEXYL ACRYLATE;Acrylic acid 1-methylcyclohexyl ester
• CAS NO: 178889-47-9
• Molecular Formula: C10H16O2
• Molecular Weight: 168.23284
• Product Categories: Medical Intermediates
• Mol File: 178889-47-9.mol

Chemical Properties

• Boiling Point: 207.5 °C at 760 mmHg
• Flash Point: 75.443 °C
• Appearance: /
• Density: 0.965 g/cm³
• Vapor Pressure: 0.225mmHg at 25°C
• Refractive Index: 1.462
• CAS DataBase Reference: 1-METHYLCYCLOHEXYL ACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHYLCYCLOHEXYL ACRYLATE(178889-47-9)
• EPA Substance Registry System: 1-METHYLCYCLOHEXYL ACRYLATE(178889-47-9)

Safety Data

• Hazardous Substances Data: 178889-47-9(Hazardous Substances Data)

Usage

Uses

Used in Polymer Industry:
1-Methylcyclohexyl Acrylate is used as a monomer for the production of polymers that require outstanding low-temperature flexibility, resilience, toughness, and weatherability.
Used in Adhesives:
1-Methylcyclohexyl Acrylate is used as a component in adhesive formulations for its good solvency and adhesive properties, contributing to the creation of strong bonds between materials.
Used in Sealants:
1-Methylcyclohexyl Acrylate is used as an ingredient in sealant formulations to provide excellent flexibility and durability, ensuring a long-lasting seal in various applications.
Used in Coatings:
1-Methylcyclohexyl Acrylate is used in the formulation of coatings to enhance their weatherability and toughness, making them suitable for outdoor applications and protection against harsh environmental conditions.
Used in Inks:
1-Methylcyclohexyl Acrylate is used in ink formulations to improve their solvency and adhesion to various surfaces, ensuring high-quality print results.

InChI:InChI=1/C10H16O2/c1-3-9(11)12-10(2)7-5-4-6-8-10/h3H,1,4-8H2,2H3

Upstream product

• 2051-76-5 acrylic acid anhydride 
• 79-10-7 acrylic acid 
• 1192-37-6 methylenecyclohexane 

Relevant articles and documents

Method for preparing linear alkyl cyclohexyl acrylate through one-pot process

The invention relates to a method for preparing linear alkyl cyclohexyl acrylate through a one-pot process. The method is characterized by comprising the following step: under inert atmosphere, enabling a Grignard reagent based on linear alkyl cyclohexano

Catalytic acryloxypalladation of vinylcycloalkanes and exo-methylene cycloalkanes. Mechanistic insights into the competition between allylic acryloxypalladation and formation of a-methylene y-butyrolactones

Acryloxypalladation of ezo-methylenecycloalkanes (three-, four-, five- and six-membered rings) and vinylcycloalkanes (three-, five- and six-membered rings) in the presence of the Pd(OAc)2/p-benzoquinone/MnC>2 catalytic system is reported. Except for the case of eio-methylenecyclopropane, this reaction provides a rapid entry to the corresponding Q-metliylene -/-butyrolactone, which essentially results from a 1,2-Markovnikov acryloxypalladation addition on the double bond. The subsequent insertion of the acrylate double bond into the carbon-palladium bond is followed by a β-elimination step. However, this reaction competes with the formation of intermediate -allyl complexes which yields the corresponding allylic acrylates. The ratio of butyrolactones to allylic acrylates is dependent on ring size. Elsevier,.