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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)-

3-(1H-imidazol-2-yl)aniline;hydrochloride

Nc1cccc(c1)c1ncc[nH]1.Cl Request for Quotation
Chemical Name: 3-(1H-imidazol-2-yl)aniline;hydrochloride
CAS Number: 1261269-04-8
Product Number: AG000RPZ(AGN-PC-0JEK2Y)
Synonyms:
MDL No: MFCD03206691
Molecular Formula: C9H10ClN3
Molecular Weight: 195.6488

Identification/Properties

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


3-(1H-Imidazol-2-yl)aniline hydrochloride is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. As a key building block in organic chemistry, this compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its imidazole ring and aniline moiety allow for diverse functional group transformations, making it a useful starting material in the preparation of complex molecules. Specifically, 3-(1H-Imidazol-2-yl)aniline hydrochloride is often employed in the synthesis of biologically active compounds, coordination complexes, and ligands for catalytic reactions. Its ability to undergo selective reactions and participate in important bond-forming processes makes it a crucial component in the development of new materials and therapeutic agents. In addition, its water-soluble hydrochloride salt form enhances its compatibility in aqueous reaction conditions, facilitating its use in various synthetic methodologies. Through strategic manipulation of its chemical structure, researchers can harness the synthetic utility of 3-(1H-Imidazol-2-yl)aniline hydrochloride to access a wide range of valuable compounds with diverse applications in the field of chemistry.