Pyridine, 3-(1H-imidazol-4-yl)-, dihydrochloride


Chemical Name: Pyridine, 3-(1H-imidazol-4-yl)-, dihydrochloride
CAS Number: 219121-67-2
Product Number: AG00C36Z(AGN-PC-0QYF8M)
Synonyms:
MDL No:
Molecular Formula: C8H9Cl2N3
Molecular Weight: 218.0832

Identification/Properties


Computed Properties
Molecular Weight:
218.081g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
217.017g/mol
Monoisotopic Mass:
217.017g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
127
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



3-(1H-Imidazol-5-yl)pyridine dihydrochloride, a powerful chemical reagent utilized in various chemical synthesis applications, serves as a versatile intermediate in organic chemistry. This compound plays a significant role in the construction of complex molecular structures, particularly in the development of pharmaceuticals, agrochemicals, and materials science. Its unique chemical properties make it an indispensable tool for the manipulation and modification of organic molecules, allowing for precise control over reaction pathways and product formation. In the realm of chemical synthesis, 3-(1H-Imidazol-5-yl)pyridine dihydrochloride enables chemists to access novel chemical compounds and enhance the efficiency of synthetic processes. With its diverse range of applications, this compound proves to be a valuable asset in the advancement of synthetic chemistry research and development initiatives.