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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-Indole-3-methanamine, 5-methoxy-

COc1ccc2c(c1)c(CN)c[nH]2 Request for Quotation
Chemical Name: 1H-Indole-3-methanamine, 5-methoxy-
CAS Number: 60523-82-2
Product Number: AG00EBPW(AGN-PC-0026T7)
Synonyms:
MDL No:
Molecular Formula: C10H12N2O
Molecular Weight: 176.21508

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
176.219g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
176.095g/mol
Monoisotopic Mass:
176.095g/mol
Topological Polar Surface Area:
51A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
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


The chemical compound (5-Methoxy-1H-indol-3-yl)methanamine, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its primary application lies in organic synthesis processes where it serves as a key intermediate for the production of various valuable compounds. Due to its unique structural properties, $name$ is commonly used in the pharmaceutical industry for the synthesis of complex molecules such as pharmaceutical drugs, agrochemicals, and bioactive compounds. Additionally, it is utilized in the development of novel materials, dyes, and functionalized molecules that have applications in diverse fields including medicine, agriculture, and materials science. The ability of (5-Methoxy-1H-indol-3-yl)methanamine to undergo various chemical reactions, such as nucleophilic substitutions and condensations, enables chemists to efficiently manipulate its structure and incorporate it into elaborate molecular frameworks, making it a valuable asset in chemical synthesis strategies.