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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)-

1-(4-Bromophenyl)-1H-pyrrole

Brc1ccc(cc1)n1cccc1 Request for Quotation
Chemical Name: 1-(4-Bromophenyl)-1H-pyrrole
CAS Number: 5044-39-3
Product Number: AG00D84E(AGN-PC-0WAMM1)
Synonyms:
MDL No:
Molecular Formula: C10H8BrN
Molecular Weight: 222.0812

Identification/Properties

Computed Properties
Molecular Weight:
222.085g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
220.984g/mol
Monoisotopic Mass:
220.984g/mol
Topological Polar Surface Area:
4.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
135
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 1-(4-Bromophenyl)-1H-pyrrole, also known as $name$, is a versatile building block in chemical synthesis. It is commonly utilized in organic chemistry as a key intermediate for the preparation of various functionalized compounds. With its unique structure and reactivity, $name$ serves as a valuable starting material for the synthesis of diverse organic molecules, including pharmaceuticals, agrochemicals, and materials. Its presence in the synthesis allows for the introduction of the 4-bromophenyl and pyrrole moieties into the final product, imparting specific properties and functionalities. Additionally, the ability of $name$ to participate in various chemical reactions, such as cross-coupling, cycloaddition, and functional group transformations, further expands its utility in designing complex molecular architectures. In essence, the strategic incorporation of 1-(4-Bromophenyl)-1H-pyrrole in chemical synthesis offers a pathway to tailor-made compounds with desired properties and applications.