1. Home
  2. Benzamide, 4-amino-N-methoxy-N-methyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzamide, 4-amino-N-methoxy-N-methyl-

CON(C(=O)c1ccc(cc1)N)C Request for Quotation
Chemical Name: Benzamide, 4-amino-N-methoxy-N-methyl-
CAS Number: 186252-52-8
Product Number: AG00I1QR(AGN-PC-06RB7T)
Synonyms:
MDL No:
Molecular Formula: C9H12N2O2
Molecular Weight: 180.2038

Identification/Properties

Computed Properties
Molecular Weight:
180.207g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
180.09g/mol
Monoisotopic Mass:
180.09g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
177
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Amino-N-methoxy-N-methylbenzamide, also known as AMMB, is a versatile compound widely utilized in chemical synthesis for various applications. This compound serves as a crucial building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and properties make it invaluable in the development of novel compounds with diverse functionalities.In chemical synthesis, AMMB is commonly employed as a precursor in the production of bioactive molecules and pharmaceutical intermediates. By leveraging its amino, methoxy, and methyl functional groups, chemists can introduce specific modifications to the molecular structure to tailor the properties and enhance the efficacy of the final product. AMMB's versatility allows for the creation of structurally diverse compounds with potential applications in drug discovery and development.Moreover, AMMB plays a vital role in the synthesis of complex organic molecules by serving as a key starting material in multi-step synthesis processes. Its presence in the synthetic pathway can enable the formation of intricate molecular architectures with precise control over stereochemistry and functional group placement. This strategic use of AMMB facilitates the efficient construction of advanced chemical scaffolds for various industries.Overall, 4-Amino-N-methoxy-N-methylbenzamide is a valuable tool in chemical synthesis, contributing to the development of innovative compounds and enabling the exploration of new chemical space. Its applications extend across different sectors, highlighting its significance in advancing the field of organic chemistry.