3085-68-5

Usage

Uses

Used in Chemical Industry:
N,N-Diallylacrylamide is used as a key component in the production of polymers for its ability to maintain structural integrity under different conditions.
Used in Coatings:
N,N-Diallylacrylamide is used as a coating material for its resistance to water, oil, and chemicals, providing durability and protection to surfaces.
Used in Adhesives:
N,N-Diallylacrylamide is used as an adhesive agent due to its strong bonding capabilities and resistance to environmental factors.
Used in Other Chemical Processes:
N,N-Diallylacrylamide is utilized in various chemical processes for its versatility and stability, contributing to the efficiency and effectiveness of these processes.
It is important to handle N,N-Diallylacrylamide with care, as excessive exposure or ingestion can result in adverse health effects.

InChI:InChI=1/C9H13NO/c1-4-7-10(8-5-2)9(11)6-3/h4-6H,1-3,7-8H2

Upstream product

• 814-68-6 acryloyl chloride 
• 124-02-7 diallylamine 
• 79-10-7 acrylic acid 

Downstream Products

• 143925-34-2 trans-N-Allyl-4-(bromomethyl)-3-(tosylmethyl)-2-pyrrolidone 
• 143925-34-2 cis-N-Allyl-4-(bromomethyl)-3-(tosylmethyl)-2-pyrrolidone 
• 140667-09-0 trans-1-allyl-4-methyl-3-<(phenylsulfanyl)methyl>pyrrolidin-2-one 
• 140635-91-2 trans-1-allyl-3-methyl-4-<(phenylsulfanyl)methyl>pyrrolidin-2-one 
• 140635-91-2 cis-1-allyl-3-methyl-4-<(phenylsulfanyl)methyl>pyrrolidin-2-one 
• 140635-93-4 trans-1-allyl-3,4-bis<(phenylsulfanyl)methyl>pyrrolidin-2-one 

Relevant academic research and scientific papers

Chemoselective, Stereospecific, and Living Polymerization of Polar Divinyl Monomers by Chiral Zirconocenium Catalysts

This contribution reports the first chemoselective, stereospecific, and living polymerization of polar divinyl monomers, enabled by chiral ansa-zirconocenium catalysts through an enantiomorphic-site controlled coordination-addition polymerization mechanis

Potassium Base-Catalyzed Michael Additions of Allylic Alcohols to α,β-Unsaturated Amides: Scope and Mechanistic Insights

We report herein the first KHMDS-catalyzed Michael additions of allylic alcohols to α,β-unsaturated amides through allylic isomerization. The reaction proceeds smoothly in the presence of only 5 mol% of KHMDS to afford a variety of 1,5-ketoamides in high yields. Mechanistic investigations, including experimental and computational studies, reveal that the KHMDS-catalyzed in-situ generation of the enolate from the allylic alcohol through a tunneling-assisted 1,2-hydride shift is the key to the success of this transformation. (Figure presented.).

Polymerizable compound, ink cartridge containing ink including the polymerizable compound, inkjet recording apparatus using the ink cartridge, and print formed by ink including the polymerizable compound

A polymerizable compound is provided. The polymerizable compound has two or more polymerizable functional groups in a molecule thereof, wherein one of the two or more polymerizable functional groups of the polymerizable compound is an acrylamide group having the below-mentioned formula (1). The polymerizable compound can be preferably used for inkjet ink.

DENTAL COMPOSITION

Dental composition comprising a polymerizable compound of the following formula (I):A-L(B) wherein A, L, B, and n are as defined in claim 1.

Dental composition

Dental composition comprising a polymerizable compound of the following formula (I): ???????? A-L(B)n?????(I) wherein A, L, B, and n are as defined in claim 1.

Mild stereoselective hydrohalogenation leading to (Z)-halopropenamides at room temperature

Hydroiodination of 2-propynamides leading stereoselectively to (Z)-iodopropenamides was achieved under mild conditions at room temperature by the combined use of zinc iodide and tert-butyl iodide. Similarly, the use of zinc bromide in the presence of tert

Radical Cyclisation in Heterocycle Synthesis. Part 1. Sulfanyl Radical Addition-Cyclisation of Dienylamides for Lactam Synthesis

A new method for the synthesis of five- to eight-membered lactams by sulfanyl radical mediated-cyclisation of dienylamides is described.The sulfanyl radical addition-cyclisation of the dienylamide 1 was systematically investigated under four different conditions and was found to give the cyclised lactams 2-6 in 54-79percent yield.The stereo- and regio-selectivity of sulfanyl radical addition-cyclisation was established from the preferential formation of the trans-cyclised lactam 3 and also from the substituent effects in the cyclisation of the dienylamides 11-18.The sulfanyl radical mediated addition-cyclisation was successfully applied to the construction of the six- and eight-membered lactams 28a, b.

Chemoselective Ring Construction from Unsymmetrical 1,6-Dienes via Radical Addition of Sulfonyl Halides

The sulfonyl radical-promoted cyclizations of 1,6-unsymmetrical dienes can be totally chemoselective.The addition of tosyl halides to various 1,6-dienes bearing both a nucleophilic and an electrophilic double bond clearly indicates that this attractive pr