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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, 2-(2-bromophenyl)-

Brc1ccccc1c1ncc[nH]1 Request for Quotation
Chemical Name: 1H-Imidazole, 2-(2-bromophenyl)-
CAS Number: 162356-38-9
Product Number: AG001T18(AGN-PC-0MY2EN)
Synonyms:
MDL No: MFCD08668745
Molecular Formula: C9H7BrN2
Molecular Weight: 223.0693

Identification/Properties

Properties
BP:
397.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
223.073g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
221.979g/mol
Monoisotopic Mass:
221.979g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
152
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:
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


In chemical synthesis, 2-(2-Bromophenyl)-1H-imidazole is a versatile and valuable building block commonly employed in the creation of various organic compounds. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials due to its unique reactivity and structural properties. By utilizing 2-(2-Bromophenyl)-1H-imidazole as a precursor, chemists can access a wide range of functionalized molecules through strategic transformations such as cross-coupling reactions, nucleophilic substitutions, and cyclization processes. The presence of the bromine substituent allows for further derivatization to introduce additional chemical functionalities, enhancing the diversity and complexity of the final products. With its significance in synthetic chemistry, 2-(2-Bromophenyl)-1H-imidazole continues to play a crucial role in the development of novel compounds with potential applications in various industries.