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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)-

3-[(2-methylimidazol-1-yl)methyl]-1,2,3,9-tetrahydrocarbazol-4-one

O=C1C(CCc2c1c1ccccc1[nH]2)Cn1ccnc1C Request for Quotation
Chemical Name: 3-[(2-methylimidazol-1-yl)methyl]-1,2,3,9-tetrahydrocarbazol-4-one
CAS Number: 99614-14-9
Product Number: AG01CBDV(AGN-PC-0NCC49)
Synonyms:
MDL No:
Molecular Formula: C17H17N3O
Molecular Weight: 279.33638

Identification/Properties

Computed Properties
Molecular Weight:
279.343g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
279.137g/mol
Monoisotopic Mass:
279.137g/mol
Topological Polar Surface Area:
50.7A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
413
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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 3-((2-Methyl-1H-imidazol-1-yl)methyl)-2,3-dihydro-1H-carbazol-4(9H)-one plays a crucial role in chemical synthesis as a versatile building block. Its unique structure allows for strategic incorporation into various chemical reactions to introduce specific functionalities or structural motifs in organic synthesis. This compound can serve as a key intermediate in the preparation of complex organic molecules or pharmaceutical compounds by facilitating the formation of new carbon-carbon or carbon-heteroatom bonds. The presence of the imidazole and carbazole moieties offers diverse reactivity and selectivity, making it a valuable tool for synthetic chemists in the development of novel molecules with potential applications in drug discovery, materials science, and other fields of chemical research.