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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)-

5,11-dimethyl-6H-pyrido[4,3-b]carbazol-9-ol;hydrochloride

Oc1ccc2c(c1)c1c(C)c3cnccc3c(c1[nH]2)C.Cl Request for Quotation
Chemical Name: 5,11-dimethyl-6H-pyrido[4,3-b]carbazol-9-ol;hydrochloride
CAS Number: 52238-35-4
Product Number: AG00DJNF(AGN-PC-0JMW8D)
Synonyms:
MDL No:
Molecular Formula: C17H15ClN2O
Molecular Weight: 298.7668

Identification/Properties

Properties
MP:
>223ºC (dec.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
298.77g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
298.087g/mol
Monoisotopic Mass:
298.087g/mol
Topological Polar Surface Area:
48.9A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
374
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 5,11-Dimethyl-6H-pyrido[4,3-b]carbazol-9-ol hydrochloride is commonly utilized in chemical synthesis as a key building block for the development of novel pharmaceuticals and organic compounds. Its unique molecular structure and reactivity make it a valuable tool in the creation of complex molecules through various synthetic routes. Specifically, this compound can serve as a precursor for the synthesis of biologically active compounds, including potential drug candidates. Its incorporation in chemical reactions can enable the formation of intricate carbon-carbon and carbon-nitrogen bonds, leading to the production of diverse molecular architectures with specific functionalities. By leveraging the properties of 5,11-Dimethyl-6H-pyrido[4,3-b]carbazol-9-ol hydrochloride in chemical synthesis, researchers can innovate and explore new avenues in drug discovery and material science.