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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)-

Acetamide, 2-amino-N-methyl-

CNC(=O)CN Request for Quotation
Chemical Name: Acetamide, 2-amino-N-methyl-
CAS Number: 22356-89-4
Product Number: AG003931(AGN-PC-0D7ZUR)
Synonyms:
MDL No: MFCD06375945
Molecular Formula: C3H8N2O
Molecular Weight: 88.1084

Identification/Properties

Computed Properties
Molecular Weight:
88.11g/mol
XLogP3:
-1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
88.064g/mol
Monoisotopic Mass:
88.064g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
52.8
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-N-methyl-acetamide, also known as N-methyl-2-aminopropanamide, is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique chemical structure and reactivity make it an essential component in the synthesis of a wide range of organic compounds.In chemical synthesis, 2-Amino-N-methyl-acetamide plays a crucial role as a precursor in the formation of complex molecules. It can undergo various reactions such as acylation, alkylation, and condensation to introduce functional groups or modify existing molecular structures. The presence of an amino group and a methyl group in its structure enables it to participate in diverse synthetic pathways, allowing for the creation of intricate chemical compounds with specific properties and functionalities.Moreover, 2-Amino-N-methyl-acetamide is commonly employed as a protecting group in peptide synthesis. By temporarily masking reactive functional groups in amino acids, this compound helps in controlling the sequence of peptide bond formation and protecting delicate chemical moieties from unwanted reactions during the synthesis process. This protective role facilitates the precise assembly of peptides and proteins with high purity and efficiency.Overall, the application of 2-Amino-N-methyl-acetamide in chemical synthesis is fundamental for the creation of a wide array of organic molecules with pharmaceutical, agricultural, and industrial significance. Its versatility and reactivity make it an indispensable tool for chemists working in various fields of organic chemistry and drug discovery.