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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-Pyrido[3,4-b]indole, 2,3,4,9-tetrahydro-6-methoxy-

COc1ccc2c(c1)c1CCNCc1[nH]2 Request for Quotation
Chemical Name: 1H-Pyrido[3,4-b]indole, 2,3,4,9-tetrahydro-6-methoxy-
CAS Number: 20315-68-8
Product Number: AG0028PB(AGN-PC-0JK61E)
Synonyms:
MDL No:
Molecular Formula: C12H14N2O
Molecular Weight: 202.2524

Identification/Properties

Properties
MP:
219-222 °C
BP:
388.6 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
202.257g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
202.111g/mol
Monoisotopic Mass:
202.111g/mol
Topological Polar Surface Area:
37A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
234
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole, also known as $name$, is a versatile compound used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals due to its structural features and reactivity.In chemical synthesis, 6-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole acts as a key intermediate in the production of biologically active compounds. Its substituted pyridoindole core provides a platform for further functionalization through various chemical reactions, such as halogenation, alkylation, acylation, and Suzuki cross-coupling reactions. These versatile synthetic routes allow for the creation of structurally diverse molecules with potential pharmacological or agricultural applications.Moreover, the presence of the methoxy group at the 6th position of the pyridoindole ring imparts specific properties to the molecule, influencing its solubility, stability, and biological activity in the final products. Through strategic modifications and derivatizations of this moiety, chemists can tailor the compound's physicochemical and biological characteristics to suit specific application requirements in drug discovery, material science, or other research fields.Overall, 6-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole plays a crucial role in chemical synthesis by serving as a versatile and valuable starting material for the construction of diverse chemical entities with potential therapeutic or industrial significance.