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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)-

2H-Benzimidazol-2-one, 1,3-dihydro-4-hydroxy-

O=c1[nH]c2c([nH]1)cccc2O Request for Quotation
Chemical Name: 2H-Benzimidazol-2-one, 1,3-dihydro-4-hydroxy-
CAS Number: 69053-50-5
Product Number: AG00FGHU(AGN-PC-00K4DM)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O2
Molecular Weight: 150.1347

Identification/Properties

Computed Properties
Molecular Weight:
150.137g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
150.043g/mol
Monoisotopic Mass:
150.043g/mol
Topological Polar Surface Area:
61.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
183
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

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Chemical Structure


4-Hydroxy-1H-benzo[d]imidazol-2(3H)-one, also known as 2-Hydroxybenzimidazole, is a versatile compound widely used in chemical synthesis. Its hydroxyl group makes it a valuable building block in various organic reactions. In organic synthesis, 4-Hydroxy-1H-benzo[d]imidazol-2(3H)-one is commonly employed as a nucleophile in the formation of C-C and C-N bonds. It can react with electrophiles such as alkyl halides or acyl chlorides to form new carbon-carbon or carbon-nitrogen bonds. This reactivity makes it a crucial component in the preparation of biologically active compounds, pharmaceuticals, and agrochemicals.Additionally, 4-Hydroxy-1H-benzo[d]imidazol-2(3H)-one can also act as a chelating ligand in coordination chemistry. Its ability to coordinate with metal ions provides a means to synthesize metal complexes with specific properties and applications, such as catalysts for organic transformations or materials for electronic devices.Overall, the unique reactivity of 4-Hydroxy-1H-benzo[d]imidazol-2(3H)-one makes it a valuable tool in chemical synthesis, enabling the creation of diverse molecular structures with potential applications in various fields of science and technology.