1. Home
  2. 2-methoxy-5-nitropyridin-4-amine

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-methoxy-5-nitropyridin-4-amine

COc1ncc(c(c1)N)[N+](=O)[O-] Request for Quotation
Chemical Name: 2-methoxy-5-nitropyridin-4-amine
CAS Number: 127356-38-1
Product Number: AG000WXO(AGN-PC-002GML)
Synonyms:
MDL No:
Molecular Formula: C6H7N3O3
Molecular Weight: 169.1381

Identification/Properties

Computed Properties
Molecular Weight:
169.14g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
169.049g/mol
Monoisotopic Mass:
169.049g/mol
Topological Polar Surface Area:
94A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
170
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Methoxy-5-nitropyridin-4-amine, also known as $name$, serves as a crucial intermediate in chemical synthesis processes due to its unique chemical properties. This compound plays a vital role in the development of various pharmaceuticals, agrochemicals, and organic materials.In chemical synthesis, $name$ acts as a versatile building block for the creation of more complex molecules. Its nitro and amino groups can undergo a wide range of chemical reactions, enabling the formation of diverse chemical structures. By strategically modifying these functional groups, chemists can fine-tune the properties of the final compounds synthesized.One key application of 2-Methoxy-5-nitropyridin-4-amine lies in its use as a precursor in the synthesis of various heterocyclic compounds. These compounds are essential in drug discovery and development, as they often exhibit potent biological activities. Additionally, $name$ can be employed in the synthesis of dyes, pigments, and other specialty chemicals, highlighting its importance in industrial processes.Overall, the strategic placement of functional groups in 2-Methoxy-5-nitropyridin-4-amine makes it a valuable tool in chemical synthesis, enabling the efficient construction of complex molecules with diverse applications.