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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-Pyridinamine, 4-ethoxy-

CCOc1ccnc(c1)N Request for Quotation
Chemical Name: 2-Pyridinamine, 4-ethoxy-
CAS Number: 52311-20-3
Product Number: AG003GF5(AGN-PC-0JWI96)
Synonyms:
MDL No: MFCD01646350
Molecular Formula: C7H10N2O
Molecular Weight: 138.1671

Identification/Properties

Properties
MP:
119-120℃
BP:
270.5°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
138.17g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
138.079g/mol
Monoisotopic Mass:
138.079g/mol
Topological Polar Surface Area:
48.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
97.6
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-4-ethoxypyridine, a versatile chemical compound, serves as a valuable building block in the realm of chemical synthesis. With its unique structure and properties, this compound is widely employed in various synthetic processes to create a diverse array of pharmaceuticals, agrochemicals, and specialty chemicals. Its significance lies in its ability to participate in key transformations, such as nucleophilic substitution, condensation reactions, and heterocyclic synthesis. In the pharmaceutical industry, 2-Amino-4-ethoxypyridine plays a crucial role in the synthesis of new drug candidates, contributing to the development of novel treatments for a range of medical conditions. Moreover, its utility extends to the creation of advanced materials and catalysts, showcasing its importance in driving innovation across different sectors of the chemical industry.