1. Home
  2. 1H-Imidazole-1-butanamine, 4-(3-pyridinyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1H-Imidazole-1-butanamine, 4-(3-pyridinyl)-

NCCCCn1cnc(c1)c1cccnc1 Request for Quotation
Chemical Name: 1H-Imidazole-1-butanamine, 4-(3-pyridinyl)-
CAS Number: 173838-63-6
Product Number: AG001Z7H(AGN-PC-0NEX57)
Synonyms:
MDL No:
Molecular Formula: C12H16N4
Molecular Weight: 216.2822

Identification/Properties

Properties
BP:
455.957°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-(4-(Pyridin-3-yl)-1H-imidazol-1-yl)butan-1-amine is a versatile compound commonly used in chemical synthesis due to its unique structure and reactivity. In organic synthesis, this compound serves as a valuable building block for the construction of various biologically active molecules and pharmaceutical intermediates. Its functional groups allow for selective modifications and derivatizations, making it a key component in the design and production of novel compounds. Specifically, 4-(4-(Pyridin-3-yl)-1H-imidazol-1-yl)butan-1-amine finds applications in the development of drug candidates, agrochemicals, and materials science research. Additionally, its presence in the chemical toolbox enables chemists to access diverse chemical space and explore new synthetic routes for target molecules.