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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, 5-fluoro-3-methyl-

Fc1ccc2c(c1)c(C)c[nH]2 Request for Quotation
Chemical Name: 1H-Indole, 5-fluoro-3-methyl-
CAS Number: 392-13-2
Product Number: AG00I7QJ(AGN-PC-0NLBUK)
Synonyms:
MDL No:
Molecular Formula: C9H8FN
Molecular Weight: 149.1649

Identification/Properties

Computed Properties
Molecular Weight:
149.168g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
149.064g/mol
Monoisotopic Mass:
149.064g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-3-methylindole is a versatile compound widely used in chemical synthesis for its unique reactivity and properties. In organic chemistry, this compound serves as a valuable building block for the preparation of various biologically active molecules and pharmaceutical intermediates. Its fluorine substituent enhances its nucleophilicity, making it a valuable tool in cross-coupling reactions and other transformation processes. Moreover, the presence of a methyl group at the 3-position provides steric influences that can be strategically utilized in the synthesis of complex organic molecules. With its potential to undergo diverse functional group transformations, 5-Fluoro-3-methylindole offers chemists a valuable platform for the development of new synthetic methodologies and the construction of intricate molecular architectures.