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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-4-methanamine

NCc1cccc2c1cc[nH]2 Request for Quotation
Chemical Name: 1H-Indole-4-methanamine
CAS Number: 3468-18-6
Product Number: AG00BXCX(AGN-PC-0JP4VT)
Synonyms:
MDL No:
Molecular Formula: C9H10N2
Molecular Weight: 146.1891

Identification/Properties

Computed Properties
Molecular Weight:
146.193g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
146.084g/mol
Monoisotopic Mass:
146.084g/mol
Topological Polar Surface Area:
41.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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 use of (1H-Indol-4-yl)methanamine in chemical synthesis is invaluable due to its unique chemical structure and reactivity. This compound serves as a versatile building block for the synthesis of various pharmaceuticals, agrochemicals, and materials with specific properties. Its indole moiety provides a rich source of aromaticity and functional groups for further derivatization. In organic synthesis, (1H-Indol-4-yl)methanamine can undergo a plethora of chemical reactions such as nucleophilic substitution, reduction, and coupling reactions to form complex molecular structures. Its incorporation into drug design can lead to the development of novel therapeutics targeting specific biological pathways. This compound also finds applications in the synthesis of fluorescent dyes, polymer materials, and natural product analogs. The versatility of (1H-Indol-4-yl)methanamine makes it a valuable tool for researchers and chemists seeking to explore new frontiers in chemical synthesis.