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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Propenamide, N-(methoxymethyl)-2-methyl-

COCNC(=O)C(=C)C Request for Quotation
Chemical Name: 2-Propenamide, N-(methoxymethyl)-2-methyl-
CAS Number: 3644-12-0
Product Number: AG00C6YU(AGN-PC-0JLQJJ)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Computed Properties
Molecular Weight:
129.159g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
129.079g/mol
Monoisotopic Mass:
129.079g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
120
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(methoxymethyl)methacrylamide is a versatile compound widely used in chemical synthesis due to its unique reactivity and properties. As a key building block in organic chemistry, this amide derivative plays a critical role in the creation of various polymers and materials. With its methoxymethyl group providing stability and protection to the reactive methacrylamide functionality, this compound enables precise control over polymerization reactions, leading to the formation of tailored products with specific properties. By incorporating N-(methoxymethyl)methacrylamide into polymerization processes, researchers can manipulate the structure and performance of resulting materials for a wide range of applications, from coatings and adhesives to biomaterials and drug delivery systems. The versatility and reliability of N-(methoxymethyl)methacrylamide make it an indispensable tool in the realm of chemical synthesis, facilitating the development of innovative solutions in various industries.