10196-75-5 Usage
General Description
N-[(diethylamino)methyl]methacrylamide, also known as DMAEMA, is a chemical compound with the molecular formula C9H18N2O. It is a widely-used monomer in the production of polymers, particularly in the field of organic synthesis and polymer chemistry. DMAEMA is known for its ability to undergo free radical polymerization, making it valuable in the formation of various types of polymers, including copolymers, homopolymers, and graft polymers. It also has applications in industries such as adhesives, coatings, and biomedical materials. Additionally, DMAEMA is used as a stabilizer in emulsion polymerization processes. However, it is important to handle DMAEMA with caution, as it is considered hazardous and should be used in accordance with proper safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 10196-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,9 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10196-75:
(7*1)+(6*0)+(5*1)+(4*9)+(3*6)+(2*7)+(1*5)=85
85 % 10 = 5
So 10196-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2O/c1-5-11(6-2)7-10-9(12)8(3)4/h3,5-7H2,1-2,4H3,(H,10,12)
10196-75-5Relevant articles and documents
Synthesis of: N -[(dialkylamino)methyl]acrylamides and N -[(dialkylamino)methyl]methacrylamides from Schiff base salts: Useful building blocks for smart polymers
Alzahrani, Abdullah,Mirallai, Styliana I.,Chalmers, Benjamin A.,McArdle, Patrick,Aldabbagh, Fawaz
, p. 4108 - 4116 (2018)
The traditional thermal Mannich reaction is unsuitable for preparing polymerizable N-methylene amino substituted acrylamides and methacrylamides. Herein we provide a facile multi-gram high yield synthesis of these monomeric precursors to stimuli-responsive polymers by the addition of acrylamides and methacrylamides onto in situ generated or freshly isolated methylene Schiff base (iminium) salts. The X-ray crystal structure of the hydrated iminium salt, 1-(hydroxymethyl)azocan-1-ium chloride and monomer·HCl salt (N-[(azocan-1-yl)methyl]prop-2-enamide hydrochloride) is described.
