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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-1-(2-hydroxyethyl)-

OCCn1c(=O)[nH]c2c1cccc2 Request for Quotation
Chemical Name: 2H-Benzimidazol-2-one, 1,3-dihydro-1-(2-hydroxyethyl)-
CAS Number: 63388-01-2
Product Number: AG00IB7D(AGN-PC-0L6CBQ)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O2
Molecular Weight: 178.1879

Identification/Properties

Computed Properties
Molecular Weight:
178.191g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
178.074g/mol
Monoisotopic Mass:
178.074g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
208
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#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2-Hydroxyethyl)-1H-benzo[d]imidazol-2(3H)-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable building block in organic chemistry.In chemical synthesis, $name$ serves as a key intermediate in the production of pharmaceutical compounds, agrochemicals, and specialty chemicals. Its hydroxyethyl group allows for easy derivatization, enabling the introduction of various functional groups to tailor the molecule for specific applications.$name$ is particularly valuable in the synthesis of heterocyclic compounds due to its benzoimidazole backbone. This heterocyclic motif is commonly found in pharmaceutical agents, offering biological activity and structural diversity. By incorporating $name$ into synthetic routes, chemists can access a diverse array of heterocyclic derivatives with potential pharmacological properties.Furthermore, the presence of the hydroxyl group in $name$ enables hydrogen bonding interactions, making it a useful ligand in coordination chemistry and catalysis. Its ability to form complexes with transition metals opens up possibilities for designing new catalysts for organic transformations.Overall, the application of 1-(2-Hydroxyethyl)-1H-benzo[d]imidazol-2(3H)-one in chemical synthesis highlights its importance as a versatile building block with significant potential for innovation and discovery in the field of organic chemistry.