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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)-

methyl 7-methyl-1H-indole-3-carboxylate

COC(=O)c1c[nH]c2c1cccc2C Request for Quotation
Chemical Name: methyl 7-methyl-1H-indole-3-carboxylate
CAS Number: 773134-49-9
Product Number: AG005NPW(AGN-PC-07QVCT)
Synonyms:
MDL No:
Molecular Formula: C11H11NO2
Molecular Weight: 189.2105

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
189.214g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
189.079g/mol
Monoisotopic Mass:
189.079g/mol
Topological Polar Surface Area:
42.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
229
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


Methyl 7-methyl-1H-indole-3-carboxylate is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a key building block for the synthesis of various indole derivatives with diverse applications.One of the primary applications of Methyl 7-methyl-1H-indole-3-carboxylate is in the pharmaceutical industry. It is commonly employed in the synthesis of pharmaceutical drugs, especially those targeting neurological disorders and cancer. The indole moiety present in this compound plays a crucial role in modulating biological activity, making it an essential intermediate in drug discovery and development.Furthermore, Methyl 7-methyl-1H-indole-3-carboxylate is utilized in the synthesis of agrochemicals and specialty chemicals. Its structural flexibility allows for the introduction of different functional groups, enabling chemists to tailor the properties of the final products for specific applications. This compound's versatility and ease of modification make it a valuable tool in the design and development of novel compounds with desired properties.Overall, Methyl 7-methyl-1H-indole-3-carboxylate is a fundamental building block in chemical synthesis, offering a wide range of applications in various industries, including pharmaceuticals, agrochemicals, and specialty chemicals. Its significance lies in its ability to serve as a precursor for the synthesis of complex molecules with diverse biological and chemical activities.