2555-13-7

Basic information

• Product Name: N-ALLYLACRYLAMIDE
• Synonyms: N-ALLYLACRYLAMIDE;N-2,2-propenyl-2-Propenamide;2-Propenamide, N-2-propenyl-;N-prop-2-enylprop-2-enamide;NSC 20946
• CAS NO: 2555-13-7
• Molecular Formula: C₆H₉NO
• Molecular Weight: 111.14
• Product Categories: monomer
• Mol File: 2555-13-7.mol

Chemical Properties

• Boiling Point: 120-123°C 19mm
• Flash Point: 129.5 °C
• Appearance: /
• Density: 0.898 g/cm³
• Vapor Pressure: 0.0386mmHg at 25°C
• Refractive Index: 1.4874 (589.3 nm 20℃)
• PKA: 14.69±0.46(Predicted)
• CAS DataBase Reference: N-ALLYLACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-ALLYLACRYLAMIDE(2555-13-7)
• EPA Substance Registry System: N-ALLYLACRYLAMIDE(2555-13-7)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 2555-13-7(Hazardous Substances Data)

Usage

Uses

Used in Polymer Production:
N-Allylacrylamide is used as a monomer in the production of polymers and copolymers for various applications due to its reactive properties that facilitate the formation of polymer chains.
Used in Adhesive Manufacturing:
In the adhesive industry, N-Allylacrylamide is used as a component in the formulation of adhesives to enhance their bonding properties and durability.
Used in Coating Industry:
N-Allylacrylamide is utilized as a key ingredient in the development of coatings, contributing to their performance characteristics such as adhesion, flexibility, and resistance to environmental factors.
Used in Personal Care Products:
Within the personal care sector, N-Allylacrylamide serves as an ingredient in the creation of various products, potentially improving their consistency, texture, and performance on application. However, its use in this industry must be carefully managed to avoid allergic reactions and skin sensitization in consumers.

InChI:InChI=1/C6H9NO/c1-3-5-7-6(8)4-2/h3-4H,1-2,5H2,(H,7,8)

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 107-11-9 1-amino-2-propene 
• 107-13-1 acrylonitrile 
• 762-72-1 allyl-trimethyl-silane 
• 814-68-6 acryloyl chloride 
• 79-10-7 acrylic acid 
• 74-86-2 acetylene 

Downstream Products

• 4031-15-6 3-pyrrolin-2-one 
• 1418218-19-5 N-acryloyl-N-allyl-2-iodobenzamide 
• 5285-74-5 4-tolyl thiocyanate 
• 5285-87-0 phenyl thiocyanate 
• 5285-90-5 4-thiocyanatoanisole 

Relevant articles and documents

A facile approach to α,β-unsaturated lactams by ring-closing metathesis

[MediaObject not available: see fulltext.]A facile and efficient strategy for the synthesis of α,β-unsaturated lactams through ring-closing metathesis of easily prepared diene amides is being reported here. Reaction conditions were optimized for metathetic cyclization of diene amides to obtain five- to sevenmembered unsubstituted and β-substituted α,β-unsaturated lactams in good to excellent yield.

N-Substituted tertiary and O-substituted quaternary carbon stereogenic centers by site-, diastereo- and enantioselective vinylogous Mannich reactions

A readily accessible small-molecule phosphine, derived from commercially available starting materials such as an enantiomerically pure amino acid, serves as the precursor to a Ag-based chiral complex that can be prepared and used in situ to promote a vari

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.

Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein

A series of 5-substituted 2-pyrrolidinones was synthesized through a one-pot ruthenium alkylidene-catalyzed tandem RCM/isomerization/nucleophilic addition sequence. The intermediates resulting from RCM/isomerization showed reactivity toward electrophiles in aldol condensation reactions which provided a new entry for the total synthesis of the antileukemic natural product violacein.

New Allylation Reaction using Allylmetal (Group IVb) Compounds: Synthesis of N-Allylamides

Reaction of allylsilanes 1a and 1d or allylstannane 1b with thallium(III) salts in nitriles such as acetonitrile, acrylonitrile, propionitrile, and benzonitrile afforded the corresponding N-allylamides.Thus, umpolung of reactivity of allylsilane and allylstannane has been established.Keywords-umpolung of reactivity; allylsilane; allylstannane; N-allylamide; thallium(III) salt; nitrile