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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)-

Phenol, 4-(1H-imidazol-2-yl)-

Oc1ccc(cc1)c1ncc[nH]1 Request for Quotation
Chemical Name: Phenol, 4-(1H-imidazol-2-yl)-
CAS Number: 15548-89-7
Product Number: AG001NYH(AGN-PC-0O4FME)
Synonyms:
MDL No: MFCD08668843
Molecular Formula: C9H8N2O
Molecular Weight: 160.1726

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
160.176g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
160.064g/mol
Monoisotopic Mass:
160.064g/mol
Topological Polar Surface Area:
48.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
144
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#:
-
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(1H-Imidazol-2-yl)phenol, commonly known as $name$, is a versatile compound widely used in chemical synthesis. Due to its unique molecular structure, $name$ serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, $name$ plays a crucial role as a reagent for the formation of heterocyclic compounds and complex organic molecules. Its imidazole moiety confers significant reactivity, allowing for the efficient construction of diverse chemical frameworks. Furthermore, the phenolic group in $name$ enables it to participate in important transformation reactions, such as nucleophilic substitution and aromatic coupling, facilitating the synthesis of structurally intricate compounds. Overall, the application of 4-(1H-Imidazol-2-yl)phenol in chemical synthesis showcases its versatility and importance in the development of novel chemicals and materials.