3066-71-5

Basic information

• Product Name: Cyclohexyl acrylate
• Synonyms: CYCLOHEXYL ACRYLATE;ACRYLIC ACID CYCLOHEXYL ESTER;2-propenoicacid,cyclohexylester;2-Propenoicacidcyclohexylester;sartomersr220;sr220;Cyclohexyl prop-2-enoate;Cyclohexyl acrylate, 98+%, stab. with 100ppm 4-methoxyphenol
• CAS NO: 3066-71-5
• Molecular Formula: C₉H₁₄O₂
• Molecular Weight: 154.21
• EINECS: 221-319-3
• Mol File: 3066-71-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 182-184°C
• Flash Point: 68°C
• Appearance: /
• Density: 0,975 g/cm3
• Vapor Pressure: 0.000811mmHg at 25°C
• Refractive Index: 1.4600
• BRN: 1937528
• CAS DataBase Reference: Cyclohexyl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexyl acrylate(3066-71-5)
• EPA Substance Registry System: Cyclohexyl acrylate(3066-71-5)

Safety Data

• Hazard Codes: Xi,N
• Statements: 37/38-51/53
• Safety Statements: 26-36/37/39-61-2
• RIDADR: 3082
• RTECS: AS7350000
• TSCA: Yes
• HazardClass: 9
• PackingGroup: III
• Hazardous Substances Data: 3066-71-5(Hazardous Substances Data)

Usage

General Description

Cyclohexyl acrylate is a chemical compound that consists of a cyclohexyl group and an acrylate group, and it is commonly used in the production of polymers and resins. It is a colorless liquid with a characteristic odor, and it has a molecular formula of C9H14O2. Cyclohexyl acrylate is known for its ability to polymerize and form long chains, making it useful in the manufacturing of various types of plastics and coatings. It is also used as a monomer in the production of adhesives, sealants, and coatings, and it is considered to be a versatile and important building block in the chemical industry. However, it is important to handle this chemical with care, as it can cause skin and eye irritation, and it should be stored and used in a well-ventilated area.

InChI:InChI=1/C9H14O2/c1-7(9(10)11)8-5-3-2-4-6-8/h8H,1-6H2,(H,10,11)/p-1

Upstream product

• 292638-85-8 acrylic acid methyl ester 
• 108-93-0 cyclohexanol 
• 79-10-7 acrylic acid 
• 108-85-0 1-bromocyclohexane 
• 74-86-2 acetylene 
• 814-68-6 acryloyl chloride 
• 110-83-8 cyclohexene 

Downstream Products

• 7779-17-1 (E)-cyclohexyl cinnamate 
• 103-26-4 Methyl cinnamate 
• 868754-92-1 (E)-(S)-5-tert-Butoxycarbonylamino-hex-2-enedioic acid 6-benzyl ester 1-cyclohexyl ester 
• 1014608-47-9 cyclohexyl (E)-3-(1-methylindol-2-yl)-2-propenoate 
• 1233936-99-6 cyclohexyl 3,3-diphenylacrylate 
• 7779-17-1 cinnamic acid cyclohexanol ester 
• 1233937-02-4 cyclohexyl 3,3-di-2-naphthylacrylate 
• 1233937-06-8 cyclohexyl 3,3-bis(2-methyl-5-nitrophenyl)acrylate 
• 1233937-10-4 cyclohexyl 3,3-bis(2,4-dimethoxyphenyl)acrylate 
• 1233937-12-6 cyclohexyl 3,3-bis(2-methyl-5-aminophenyl)acrylate 
• 1428346-02-4 (Z)-cyclohexyl 2-bromo-3-(phenylamino)acrylate 
• 1428346-03-5 (E)-cyclohexyl 2-bromo-3-(phenylamino)acrylate 
• 1436591-21-7 (E)-cyclohexyl 3-(1-benzoyl-1H-indol-2-yl)acrylate 
• 1476745-46-6 (Z)-cyclohexyl 3-(phenylamino)acrylate 

Relevant articles and documents

Phosphine-Catalyzed Cascade Annulation of MBH Carbonates and Diazenes: Synthesis of Hexahydrocyclopenta[c]pyrazole Derivatives

A phosphine-catalyzed cascade annulation of Morita-Baylis-Hillman (MBH) carbonates and diazenes was achieved, giving tetrahydropyrazole-fused heterocycles bearing two five-membered rings in moderate to excellent yields. The reaction underwent an unprecedented reaction mode of MBH carbonates, in which two molecules of MBH carbonates were fully merged into the ring system.

METHOD FOR PRODUCING DICARBOXYLIC ACID

A method for producing dicarboxylic acid. The method includes: subjecting a raw material system including a cyclic olefin and a lower monocarboxylic acid to an addition reaction in the presence of an addition reaction catalyst to generate an intermediate product system including cyclic carboxylic acid ester; and subjecting the intermediate product system including cyclic carboxylic acid ester to a ring-opening and oxidation reaction in the presence of an oxidant and an oxidation catalyst to generate a corresponding dicarboxylic acid product. The addition reaction in the dicarboxylic acid synthesis route achieves a high single-pass conversion rate, and the selectivity of the corresponding cyclic carboxylic acid ester is high. The addition-oxidation synthesis route achieves faster reaction rates for both the addition reaction and oxidation reaction, and high yield of corresponding dicarboxylic acid product. The addition-oxidation based synthesis route is suitable for continuous, stable and large-scale production of corresponding dicarboxylic acid product.

ZINC COMPLEX

A zinc complex characterized in exhibiting an octahedral structure and being configured from repeating units represented by general formula (I): wherein L represents a linker region, and R1 represents a C1-4 alkyl group, which can have a halogen atom.