1. Home
  2. 4-bromo-1-propylimidazole

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)-

4-bromo-1-propylimidazole

CCCn1cnc(c1)Br Request for Quotation
Chemical Name: 4-bromo-1-propylimidazole
CAS Number: 1353856-52-6
Product Number: AG00A5N4(AGN-PC-0GXB52)
Synonyms:
MDL No:
Molecular Formula: C6H9BrN2
Molecular Weight: 189.0531

Identification/Properties

Computed Properties
Molecular Weight:
189.056g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
187.995g/mol
Monoisotopic Mass:
187.995g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
87.1
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Bromo-1-propyl-1H-imidazole is a versatile compound widely used in chemical synthesis as a key building block for the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, this compound serves as a valuable intermediate in the synthesis of various biologically active molecules.In organic synthesis, 4-Bromo-1-propyl-1H-imidazole can be used to introduce the imidazole ring system into more complex molecules, providing them with specific pharmaceutical properties. Its bromo functionality allows for further derivatization through various coupling reactions, enabling the modification of the compound for specific applications.Furthermore, the propyl chain in 4-Bromo-1-propyl-1H-imidazole offers flexibility in molecular design, allowing for the manipulation of the compound's physicochemical properties. This flexibility is crucial in optimizing the bioavailability, solubility, and target specificity of the final product.Overall, the strategic incorporation of 4-Bromo-1-propyl-1H-imidazole in chemical synthesis provides synthetic chemists with a powerful tool for the development of novel compounds with potential therapeutic or agricultural applications.