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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-(1H-benzimidazol-2-yl)ethanol

CC(c1nc2c([nH]1)cccc2)O Request for Quotation
Chemical Name: 1-(1H-benzimidazol-2-yl)ethanol
CAS Number: 19018-24-7
Product Number: AG002EDC(AGN-PC-0JN0X7)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O
Molecular Weight: 162.1885

Identification/Properties

Computed Properties
Molecular Weight:
162.192g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
162.079g/mol
Monoisotopic Mass:
162.079g/mol
Topological Polar Surface Area:
48.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(1H-Benzo[d]imidazol-2-yl)ethanol, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactions. This compound serves as a key building block in the creation of various organic molecules due to its functional groups and reactivity.In chemical synthesis, $name$ is commonly employed as a nucleophilic reagent in the formation of carbon-carbon and carbon-heteroatom bonds. Its benzimidazole ring structure imparts aromaticity and electron density, making it a valuable substrate for cascade reactions and heterocyclic syntheses. Additionally, the hydroxyl group in 1-(1H-Benzo[d]imidazol-2-yl)ethanol allows for facile derivatization, enabling the attachment of different moieties to tailor the molecule for specific applications.Moreover, the presence of both basic and acidic functional groups in $name$ offers opportunities for diverse transformations, such as condensation reactions, nucleophilic substitutions, and metal-catalyzed processes. This versatility makes 1-(1H-Benzo[d]imidazol-2-yl)ethanol a valuable tool for synthesizing pharmaceuticals, agrochemicals, and specialty chemicals with enhanced efficacy and selectivity.By harnessing the chemical properties of 1-(1H-Benzo[d]imidazol-2-yl)ethanol, researchers and chemists can efficiently construct complex molecular scaffolds and probe new reaction pathways, paving the way for innovative advancements in drug discovery, material science, and organic synthesis.