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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-[(4-chlorophenyl)methyl]imidazol-2-yl]methanol

OCc1nccn1Cc1ccc(cc1)Cl Request for Quotation
Chemical Name: [1-[(4-chlorophenyl)methyl]imidazol-2-yl]methanol
CAS Number: 175203-53-9
Product Number: AG0020J1(AGN-PC-0KKZE6)
Synonyms:
MDL No:
Molecular Formula: C11H11ClN2O
Molecular Weight: 222.6708

Identification/Properties

Computed Properties
Molecular Weight:
222.672g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
222.056g/mol
Monoisotopic Mass:
222.056g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
195
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (1-(4-Chlorobenzyl)-1H-imidazol-2-yl)methanol, often referred to as $name$, is widely utilized in chemical synthesis for its versatile applications. This molecule serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and organic compounds.In chemical synthesis, $name$ plays a crucial role as a key intermediate in the creation of diverse products. Its unique structure and reactivity make it ideal for forming complex molecular structures through various reactions such as coupling, cross-coupling, and cyclization processes. By incorporating $name$ into synthetic pathways, chemists can efficiently access a range of target compounds with desired pharmacological, agricultural, or material properties.Moreover, the presence of a chlorobenzyl group in $name$ imparts specific chemical properties that can be leveraged for selective functionalization and modification. This allows for precise control over the structure and properties of the final synthesized molecules, enabling tailored design strategies in drug discovery, material science, and other fields.Overall, the application of (1-(4-Chlorobenzyl)-1H-imidazol-2-yl)methanol in chemical synthesis offers a strategic advantage to researchers and chemists seeking to develop novel compounds with tailored functions and properties. Its versatility and utility make it a valuable tool in the toolbox of modern synthetic chemistry.