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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)-

2-imidazol-1-ylethanamine;dihydrochloride

NCCn1cncc1.Cl.Cl Request for Quotation
Chemical Name: 2-imidazol-1-ylethanamine;dihydrochloride
CAS Number: 93668-43-0
Product Number: AG003EPG(AGN-PC-0NITL2)
Synonyms:
MDL No: MFCD06798214
Molecular Formula: C5H11Cl2N3
Molecular Weight: 184.0669

Identification/Properties

Properties
MP:
217 - 220 °C
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
184.064g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
183.033g/mol
Monoisotopic Mass:
183.033g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
64.7
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:
3
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


2-(1H-Imidazol-1-yl)ethanamine dihydrochloride is a versatile compound commonly used in chemical synthesis due to its unique properties and functional groups. This compound serves as a valuable building block in organic chemistry, particularly in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its imidazole moiety imparts reactivity and selectivity, making it a valuable intermediate in the preparation of various heterocyclic compounds. Additionally, the dihydrochloride salt form enhances the compound's solubility and stability, facilitating its incorporation into a wide range of synthetic pathways.