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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)-

6-Quinoxalinamine, N-(4,5-dihydro-1H-imidazol-2-yl)-

C1CN=C(N1)Nc1ccc2c(c1)nccn2 Request for Quotation
Chemical Name: 6-Quinoxalinamine, N-(4,5-dihydro-1H-imidazol-2-yl)-
CAS Number: 91147-43-2
Product Number: AG00GWLQ(AGN-PC-0N0G0D)
Synonyms:
MDL No:
Molecular Formula: C11H11N5
Molecular Weight: 213.2385

Identification/Properties

Computed Properties
Molecular Weight:
213.244g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
213.101g/mol
Monoisotopic Mass:
213.101g/mol
Topological Polar Surface Area:
62.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
278
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Quinoxalinamine, N-(4,5-dihydro-1H-imidazol-2-yl)- is a versatile compound that plays a crucial role in chemical synthesis. This compound is widely utilized as a key building block in the development of various pharmaceuticals, agrochemicals, and materials. Its unique structure and properties make it a valuable intermediate in the creation of advanced organic compounds.In chemical synthesis, 6-Quinoxalinamine, N-(4,5-dihydro-1H-imidazol-2-yl)- serves as a vital reagent for the construction of heterocyclic frameworks. Its imidazole moiety enables it to participate in a wide range of synthetic transformations, allowing for the generation of diverse molecular structures with potential biological activities. This compound is particularly valued in the pharmaceutical industry for its ability to introduce key functional groups and enhance the potency and selectivity of bioactive molecules.Furthermore, 6-Quinoxalinamine, N-(4,5-dihydro-1H-imidazol-2-yl)- finds application in the synthesis of novel ligands, catalysts, and complex organic molecules. Its versatility and reactive nature make it a valuable tool for organic chemists seeking to access complex chemical space and explore new avenues in drug discovery and material science. By leveraging the unique reactivity of this compound, researchers can design and construct sophisticated molecular architectures that have the potential to impact various fields of science and technology.