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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)-

1H-Imidazole, 4,5-dibromo-

Brc1[nH]cnc1Br Request for Quotation
Chemical Name: 1H-Imidazole, 4,5-dibromo-
CAS Number: 2302-30-9
Product Number: AG002LWM(AGN-PC-0JMXHI)
Synonyms:
MDL No:
Molecular Formula: C3H2Br2N2
Molecular Weight: 225.8694

Identification/Properties

Properties
MP:
214-216°C
BP:
388.6°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
225.871g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
225.856g/mol
Monoisotopic Mass:
223.858g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
68
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:
Signal Word:
Danger
UN#:
2928
Hazard Statements:
H301-H315-H318-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P321-P330-P332+P313-P362-P403+P233-P405-P501
Class:
6.1,8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dibromo-1H-imidazole is a versatile chemical compound that finds wide application in chemical synthesis. One key use of this compound is as a building block for the synthesis of various biologically active molecules. It serves as a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and materials with potential for medicinal and industrial applications.In chemical synthesis, 4,5-Dibromo-1H-imidazole acts as a reactive intermediate that can undergo a variety of functional group transformations such as substitution, addition, and cyclization reactions. Its unique structure and reactivity make it a valuable tool for creating complex molecular architectures with specific properties and functions.By incorporating 4,5-Dibromo-1H-imidazole into synthetic pathways, chemists can introduce the bromine functionality at specific positions within a molecule, enabling precise control over the final product's physical and chemical properties. This compound plays a crucial role in the discovery and development of new compounds with potential therapeutic, agricultural, or materials applications.Overall, the application of 4,5-Dibromo-1H-imidazole in chemical synthesis offers a strategic approach to access diverse chemical space and create novel compounds with tailored properties for various industrial and scientific purposes.