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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-4-ol, 6-methyl-

Cc1cc(O)c2c(c1)[nH]cc2 Request for Quotation
Chemical Name: 1H-Indol-4-ol, 6-methyl-
CAS Number: 61545-41-3
Product Number: AG00E9AE(AGN-PC-02T9Y7)
Synonyms:
MDL No:
Molecular Formula: C9H9NO
Molecular Weight: 147.1739

Identification/Properties

Properties
BP:
340.9±22.0°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
147.177g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
147.068g/mol
Monoisotopic Mass:
147.068g/mol
Topological Polar Surface Area:
36A^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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methyl-1H-indol-4-ol, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and functional groups. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, $name$ is commonly employed as a precursor for the construction of complex molecular structures due to its reactivity and ability to undergo various chemical transformations. Its indole ring system, combined with the hydroxyl group at position 4, enables it to participate in a range of reactions such as N-alkylation, O-acylation, and condensation reactions.One prominent application of $name$ in chemical synthesis is in the preparation of bioactive compounds and natural product derivatives. By selectively functionalizing the methyl and hydroxyl groups of $name$, chemists can introduce specific functionalities and stereochemistry necessary for the development of novel pharmaceuticals or agrochemicals with enhanced biological activities.Moreover, the presence of both electron-rich and electron-deficient sites in $name$ allows for the formation of diverse molecular scaffolds through cyclization reactions, leading to the creation of structurally complex molecules with potential therapeutic or agricultural applications.Overall, the strategic utilization of 6-Methyl-1H-indol-4-ol in chemical synthesis enables chemists to access a valuable toolbox of synthetic transformations for the efficient and controlled assembly of valuable compounds with targeted properties and functions.