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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)-

2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole;hydrochloride

N1CCc2c(C1)[nH]c1c2cccc1.Cl Request for Quotation
Chemical Name: 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole;hydrochloride
CAS Number: 58911-02-7
Product Number: AG00E9Z1(AGN-PC-0JPNSZ)
Synonyms:
MDL No:
Molecular Formula: C11H13ClN2
Molecular Weight: 208.6873

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrido[3,4-b]indole, 2,3,4,9-tetrahydro-, hydrochloride (1:1) is a versatile compound commonly used in chemical synthesis due to its unique structural properties and reactivity. This specific molecule serves as a crucial building block in the preparation of various pharmaceuticals, agrochemicals, and organic materials.In chemical synthesis, 1H-Pyrido[3,4-b]indole, 2,3,4,9-tetrahydro-, hydrochloride (1:1) acts as a key intermediate in the formation of complex organic molecules. Its structure allows for the introduction of different functional groups through various synthetic methods, making it a valuable component in creating novel compounds with desired properties.Moreover, the hydrochloride salt form of this compound provides enhanced solubility in common organic solvents, facilitating its application in different reaction conditions. By incorporating 1H-Pyrido[3,4-b]indole, 2,3,4,9-tetrahydro-, hydrochloride (1:1) into synthetic pathways, chemists can access a diverse range of molecular scaffolds and derivatives, enabling the synthesis of potential drug candidates, bioactive compounds, and advanced materials.