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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)-

Imidazo[1,2-a]pyrimidine-2-methanamine

NCc1cn2c(n1)nccc2 Request for Quotation
Chemical Name: Imidazo[1,2-a]pyrimidine-2-methanamine
CAS Number: 843609-02-9
Product Number: AG008IES(AGN-PC-0KW1H8)
Synonyms:
MDL No:
Molecular Formula: C7H8N4
Molecular Weight: 148.1652

Identification/Properties

Computed Properties
Molecular Weight:
148.169g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
148.075g/mol
Monoisotopic Mass:
148.075g/mol
Topological Polar Surface Area:
56.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
138
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Imidazo[1,2-a]pyrimidine-2-methanamine, also known as $name$, is a versatile compound widely used in various chemical synthesis processes. This compound acts as an important building block in the creation of diverse organic molecules due to its unique structural features and reactivity.In chemical synthesis, $name$ serves as a key intermediate in the production of heterocyclic compounds, pharmaceuticals, and agrochemicals. Its presence in the reaction mixture facilitates the formation of complex molecular structures through diverse synthetic routes. $name$ is particularly valued for its ability to participate in multiple types of reactions, allowing for the efficient creation of intricate chemical architectures.Furthermore, the presence of the methanamine group in the structure of $name$ enhances its utility as a versatile synthetic precursor. This functional group enables selective derivatization, enabling chemists to introduce specific substituents and functional groups into the final products, tailoring the chemical properties and biological activities of the synthesized compounds.Overall, Imidazo[1,2-a]pyrimidine-2-methanamine plays a crucial role in chemical synthesis by providing a robust foundation for the construction of diverse organic molecules with tailored characteristics and functionalities. Its strategic incorporation in synthetic pathways underscores its significance as a valuable tool for researchers and industry professionals striving to develop novel compounds with enhanced properties and applications.