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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)-

5-bromo-4-methyl-1H-benzimidazole

Brc1ccc2c(c1C)nc[nH]2 Request for Quotation
Chemical Name: 5-bromo-4-methyl-1H-benzimidazole
CAS Number: 952511-48-7
Product Number: AG00IIW2(AGN-PC-0CRY6J)
Synonyms:
MDL No:
Molecular Formula: C8H7BrN2
Molecular Weight: 211.0586

Identification/Properties

Computed Properties
Molecular Weight:
211.062g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
209.979g/mol
Monoisotopic Mass:
209.979g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-4-methyl-1H-benzo[d]imidazole, also known by its chemical formula C8H6BrN3, plays a crucial role in chemical synthesis due to its versatile applications. As a heterocyclic compound, it serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials in the field of organic chemistry. This compound is particularly valued for its ability to participate in a wide range of reactions, making it a valuable intermediate in the synthesis of complex organic molecules. Its unique structural properties make it an essential component in the development of novel compounds with diverse functionalities and biological activities. Through strategic manipulation of its chemical structure, chemists can access a plethora of derivatives with tailored properties, paving the way for innovative advancements in the field of chemical synthesis.