1,2-Ethanediamine, N-(5-nitro-2-pyridinyl)-|29602-39-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

1,2-Ethanediamine, N-(5-nitro-2-pyridinyl)-

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Chemical Name:	1,2-Ethanediamine, N-(5-nitro-2-pyridinyl)-
CAS Number:	29602-39-9
Product Number:	AG002YUY(AGN-PC-0JLNXB)
Synonyms:
MDL No:
Molecular Formula:	C7H10N4O2
Molecular Weight:	182.1799

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Properties

MP:

126-128℃(lit.)

Form:

Solid

Computed Properties

Molecular Weight:

182.183g/mol

XLogP3:

0.1

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

182.08g/mol

Monoisotopic Mass:

182.08g/mol

Topological Polar Surface Area:

96.8A^2

Heavy Atom Count:

Formal Charge:

Complexity:

170

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

2-[(2-Aminoethyl)amino]-5-nitropyridine plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and properties make it an essential component in the creation of various pharmaceuticals, dyes, and agrochemicals. This compound serves as a key intermediate in the synthesis of complex organic molecules, allowing for the modification and functionalization of the pyridine ring. By utilizing 2-[(2-Aminoethyl)amino]-5-nitropyridine, chemists can achieve precise control over the structure and properties of the final products, enabling the development of novel compounds with diverse applications in the field of organic chemistry.