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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)-

9H-Carbazole-3-carboxaldehyde, 9-(phenylmethyl)-

O=Cc1ccc2c(c1)c1ccccc1n2Cc1ccccc1 Request for Quotation
Chemical Name: 9H-Carbazole-3-carboxaldehyde, 9-(phenylmethyl)-
CAS Number: 54117-37-2
Product Number: AG003NKC(AGN-PC-0KP49E)
Synonyms:
MDL No:
Molecular Formula: C20H15NO
Molecular Weight: 285.3392

Identification/Properties

Properties
MP:
134℃
BP:
444.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
285.346g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
285.115g/mol
Monoisotopic Mass:
285.115g/mol
Topological Polar Surface Area:
22A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
389
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


9-Benzyl-9H-carbazole-3-carbaldehyde is a versatile compound widely utilized in chemical synthesis as a key intermediate in various organic reactions. Its unique chemical structure makes it an essential building block for the synthesis of complex molecules and pharmaceuticals.In organic synthesis, 9-Benzyl-9H-carbazole-3-carbaldehyde serves as a valuable starting material for the preparation of a wide range of compounds, including heterocyclic derivatives and chiral molecules. Its carbonyl group and aromatic benzyl moiety are key functional groups that allow for diverse chemical transformations, such as nucleophilic additions, reductions, and condensations. One common application of 9-Benzyl-9H-carbazole-3-carbaldehyde is in the construction of biologically active compounds and natural product synthesis. By strategically modifying its chemical structure, chemists can access new molecules with potential pharmaceutical applications. Additionally, the presence of the carbazole scaffold in this aldehyde provides opportunities for further functionalization and derivatization, enhancing its utility in medicinal chemistry and material science.Overall, the role of 9-Benzyl-9H-carbazole-3-carbaldehyde in chemical synthesis is indispensable for the efficient preparation of structurally diverse and complex molecules with valuable properties and applications in various industries.