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
• Article Data: 5

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

General Description

N-Allylacrylamide, also known as N-AcrA or N-Allylacetamide, is a chemical compound with the molecular formula C6H9NO. It is a colorless to yellow liquid with a pungent odor that is used in the production of polymers and copolymers, as well as in the manufacturing of adhesives, coatings, and personal care products. N-Allylacrylamide is considered a hazardous chemical and should be handled with care due to its potential for irritation to skin and eyes, as well as its flammability. N-ALLYLACRYLAMIDE is also known to be a skin sensitizer and may cause allergic reactions in some individuals. It is important to follow proper safety protocols when handling N-Allylacrylamide to minimize the risk of exposure and potential health hazards.

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

Upstream product

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

Downstream Products

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

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.

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.

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