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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-(triphenylmethyl)-

O=Cc1nccn1C(c1ccccc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 1H-Imidazole-2-carboxaldehyde, 1-(triphenylmethyl)-
CAS Number: 67478-50-6
Product Number: AG006G8U(AGN-PC-0JTVWS)
Synonyms:
MDL No:
Molecular Formula: C23H18N2O
Molecular Weight: 338.4018

Identification/Properties

Properties
MP:
190-193 °C
BP:
547°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
338.41g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
338.142g/mol
Monoisotopic Mass:
338.142g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
402
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Trityl-1H-imidazole-2-carbaldehyde, a versatile building block in chemical synthesis, serves as a crucial intermediate in the preparation of various compounds due to its unique reactivity and structural properties. Its application extends to the synthesis of diverse organic molecules, including pharmaceuticals, agrochemicals, and materials. The aldehyde functional group enables the compound to undergo various organic transformations, such as nucleophilic addition reactions and condensation reactions, allowing for the formation of complex structures. Furthermore, the imidazole ring confers specific reactivity and can participate in further functionalization steps, enhancing the versatility of this compound in creating a wide range of derivatives. Overall, 1-Trityl-1H-imidazole-2-carbaldehyde plays a pivotal role in organic synthesis by facilitating the efficient construction of intricate molecular architectures for diverse applications.