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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-Indol-5-ol, 4-fluoro-2-methyl-

Oc1ccc2c(c1F)cc([nH]2)C Request for Quotation
Chemical Name: 1H-Indol-5-ol, 4-fluoro-2-methyl-
CAS Number: 288385-88-6
Product Number: AG002WPV(AGN-PC-0N311S)
Synonyms:
MDL No:
Molecular Formula: C9H8FNO
Molecular Weight: 165.1643

Identification/Properties

Computed Properties
Molecular Weight:
165.167g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
165.059g/mol
Monoisotopic Mass:
165.059g/mol
Topological Polar Surface Area:
36A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
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


4-Fluoro-5-hydroxy-2-methylindole is a versatile compound widely used in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key building block in the production of various biologically active molecules. It is commonly employed as a precursor in the synthesis of pharmaceutical agents, such as anticancer drugs and antiviral medications. Additionally, 4-Fluoro-5-hydroxy-2-methylindole plays a crucial role in the development of new materials and chemical processes due to its unique reactivity and functional properties. Its strategic incorporation into organic frameworks allows for the generation of diverse molecular structures with potentially enhanced biological activities. This compound's significance in chemical synthesis lies in its ability to serve as a foundational component for the creation of novel molecules with promising applications in medicinal chemistry and beyond.