N,1-dimethylimidazol-2-amine|1083224-07-0,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)-

N,1-dimethylimidazol-2-amine

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Chemical Name:	N,1-dimethylimidazol-2-amine
CAS Number:	1083224-07-0
Product Number:	AG00HB5B(AGN-PC-07CY15)
Synonyms:
MDL No:
Molecular Formula:	C5H9N3
Molecular Weight:	111.14506

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

Computed Properties

Molecular Weight:

111.148g/mol

XLogP3:

0.3

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

111.08g/mol

Monoisotopic Mass:

111.08g/mol

Topological Polar Surface Area:

29.8A^2

Heavy Atom Count:

Formal Charge:

Complexity:

74.1

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:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

The versatile N,1-Dimethyl-1H-imidazol-2-amine plays a crucial role in chemical synthesis as a valuable building block. Its unique structure lends itself to a variety of applications in organic synthesis, particularly in the formation of complex heterocyclic compounds. This compound acts as an important precursor in various synthetic pathways, enabling chemists to access a broad range of functionalized molecules with diverse properties. With its reactivity and compatibility with a range of reagents, N,1-Dimethyl-1H-imidazol-2-amine serves as an indispensable tool for creating novel compounds and advancing research in the field of organic chemistry.