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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, 4-methyl-1-(triphenylmethyl)-

Cc1ncn(c1)C(c1ccccc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 1H-Imidazole, 4-methyl-1-(triphenylmethyl)-
CAS Number: 82594-80-7
Product Number: AG008K6G(AGN-PC-0JTVWT)
Synonyms:
MDL No:
Molecular Formula: C23H20N2
Molecular Weight: 324.4183

Identification/Properties

Computed Properties
Molecular Weight:
324.427g/mol
XLogP3:
5.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
324.163g/mol
Monoisotopic Mass:
324.163g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
357
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


4-Methyl-1-trityl-1H-imidazole is a versatile compound widely utilized in chemical synthesis processes. Its primary application lies in its role as a potent building block for the construction of various organic molecules. Due to its unique structure and reactivity, this compound serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. 4-Methyl-1-trityl-1H-imidazole is particularly valued for its ability to participate in diverse chemical reactions, including nucleophilic substitutions, acylations, and condensations. Its presence in synthesis routes enables the efficient assembly of complex molecular structures with high precision and selectivity. Additionally, this compound exhibits excellent stability under a wide range of reaction conditions, making it a valuable tool for chemists engaged in the development of novel compounds and materials. Overall, the versatility and reliability of 4-Methyl-1-trityl-1H-imidazole make it an indispensable component in the arsenal of synthetic chemists aiming to create innovative and impactful products.