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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)-

1H-Imidazole-2-carboxaldehyde, 1-(phenylmethyl)-

O=Cc1nccn1Cc1ccccc1 Request for Quotation
Chemical Name: 1H-Imidazole-2-carboxaldehyde, 1-(phenylmethyl)-
CAS Number: 10045-65-5
Product Number: AG000211(AGN-PC-0JMQJO)
Synonyms:
MDL No:
Molecular Formula: C11H10N2O
Molecular Weight: 186.2099

Identification/Properties

Computed Properties
Molecular Weight:
186.214g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
186.079g/mol
Monoisotopic Mass:
186.079g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
190
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


1-Benzyl-1H-imidazole-2-carbaldehyde, also known as $name$, is a versatile organic compound commonly utilized in chemical synthesis due to its unique reactivity and structural properties. This compound serves as a valuable building block in the preparation of various biologically active molecules, pharmaceuticals, and advanced materials.One of the primary applications of 1-Benzyl-1H-imidazole-2-carbaldehyde is its use as a key intermediate in the synthesis of heterocyclic compounds. By reacting with different nucleophiles and electrophiles, this compound can undergo various transformations to yield a wide range of derivatives with diverse functional groups. These derivatives exhibit important biological activities and are essential precursors for drug discovery and development.Furthermore, 1-Benzyl-1H-imidazole-2-carbaldehyde plays a crucial role in the construction of complex organic molecules with specific stereochemical configurations. Its ability to participate in various multistep reactions, such as condensation, reduction, and cyclization, enables chemists to access structurally intricate compounds efficiently. This compound's reactivity and versatility make it an indispensable tool in the synthesis of natural products, fine chemicals, and advanced organic materials.In summary, 1-Benzyl-1H-imidazole-2-carbaldehyde is a valuable compound in chemical synthesis, offering diverse synthetic pathways and enabling the efficient preparation of complex organic molecules with important biological and pharmaceutical applications.