20069-66-3

Basic information

• Product Name: ALPHA-NAPHTHYL ACRYLATE
• Synonyms: ALPHA-NAPHTHYL ACRYLATE;2-Propenoicacid,1-naphthalenylester;1-Naphthyl acrylate;1-Naphthyl propenoate;Acrylic acid 1-naphthyl ester
• CAS NO: 20069-66-3
• Molecular Formula: C₁₃H₁₀O₂
• Molecular Weight: 198.22
• Product Categories: monomer
• Mol File: 20069-66-3.mol
• Article Data: 9

Chemical Properties

• Flash Point: >110°C
• Appearance: /
• Density: 1.147
• CAS DataBase Reference: ALPHA-NAPHTHYL ACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ALPHA-NAPHTHYL ACRYLATE(20069-66-3)
• EPA Substance Registry System: ALPHA-NAPHTHYL ACRYLATE(20069-66-3)

Safety Data

• Statements: 36
• Safety Statements: 26
• Hazardous Substances Data: 20069-66-3(Hazardous Substances Data)

Usage

General Description

Alpha-naphthyl acrylate is a chemical compound with the molecular formula C12H10O2. It is a colorless to light yellow liquid that is commonly used as a monomer in the production of polymers and other substances. Alpha-naphthyl acrylate is also used in the manufacture of UV-curable coatings, adhesives, and inks. It is known for its high reactivity and ability to polymerize easily, making it a valuable ingredient in various industrial processes. However, it should be handled with caution, as it can irritate the skin and eyes, and may be harmful if swallowed or inhaled.

Upstream product

• 90-15-3 α-naphthol 
• 814-68-6 acryloyl chloride 
• 79-10-7 acrylic acid 
• 1033462-77-9 tert-butyl acryloyl carbonate 

Downstream Products

• 17324-17-3 trans-3-methyl-1,4-diphenylazetidin-2-one 
• 1620141-60-7 (S)-naphthalen-1-yl 4-nitro-5-phenyl-4-(phenylsulfonyl)pentanoate 

Relevant articles and documents

Clay anti-swelling agent for acidifying acid in high-temperature oil field

The invention relates to the technical field of oilfield development, in particular to a clay anti-swelling agent for high temperature oilfield acidification. The clay anti-swelling agent is preparedby: reacting 1-naphthol with acrylic acid to generate na

CARBOXYLIC ACID ESTER PRODUCTION METHOD

Provided is a production method whereby corresponding carboxylic acid esters can be obtained from a variety of carboxylic acids at a high yield, even under conditions using a simple reaction operation and little catalyst and even if the amount of substrate used is theoretical. A production method for carboxylic acid ester, whereby a prescribed diester dicarbonate, carboxylic acid, and alcohol are reacted in the presence of at least one type of magnesium compound and at least one type of alkali metal compound.

1,4-Diazabicyclo[2.2.2]octane-Promoted Aminotrifluoromethylthiolation of α,β-Unsaturated Carbonyl Compounds: N-Trifluoromethylthio-4-nitrophthalimide Acts as Both the Nitrogen and SCF3 Sources

A novel difunctionalization reaction is described. It uses N-trifluoromethylthio-4-nitrophthalimide as the reagent, which serves as both the nitrogen and SCF3 sources. In the presence of DABCO (1,4-diazabicyclo[2.2.2]octane), the nitrogen and SCF3 groups can be incorporated into α,β-unsaturated carbonyl compounds easily and give versatile β-amino ketones and esters in good yields. This difunctionalization reaction features mild reaction conditions, high atom-economy, and efficient access to α-SCF3 amino acids.