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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-ethanamine, 7-methoxy-

NCCc1c[nH]c2c1cccc2OC Request for Quotation
Chemical Name: 1H-Indole-3-ethanamine, 7-methoxy-
CAS Number: 2436-04-6
Product Number: AG00BD3F(AGN-PC-0JKD98)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O
Molecular Weight: 190.24166

Identification/Properties

Computed Properties
Molecular Weight:
190.246g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
190.111g/mol
Monoisotopic Mass:
190.111g/mol
Topological Polar Surface Area:
51A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
186
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


2-(7-Methoxy-1H-indol-3-yl)ethan-1-amine, also known as $name$, is a crucial compound extensively employed in chemical synthesis processes. This compound serves as a versatile building block in various synthetic routes, particularly in the pharmaceutical and agrochemical industries. With its unique structural characteristics, $name$ plays a pivotal role in the creation of diverse molecular structures and complex organic compounds. Its presence enables the modification of functional groups, leading to the production of novel chemical entities with enhanced biological activities and properties. In organic synthesis, $name$ acts as a key intermediate, facilitating the formation of numerous biologically active molecules and innovative materials. Its strategic use in chemical transformations underscores its significance as a valuable tool for synthesizing a wide range of compounds with potential applications in drug discovery, materials science, and chemical research.