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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-3-carboxaldehyde, 6-methoxy-

COc1ccc2c(c1)[nH]cc2C=O Request for Quotation
Chemical Name: 1H-Indole-3-carboxaldehyde, 6-methoxy-
CAS Number: 70555-46-3
Product Number: AG00IC2R(AGN-PC-0JXWJM)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2
Molecular Weight: 175.1840

Identification/Properties

Computed Properties
Molecular Weight:
175.187g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
175.063g/mol
Monoisotopic Mass:
175.063g/mol
Topological Polar Surface Area:
42.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
195
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methoxy-1H-indole-3-carbaldehyde is a versatile compound frequently utilized in chemical synthesis due to its unique structural properties. This aldehyde derivative plays a crucial role in various organic reactions, especially in the pharmaceutical and agrochemical industries. One of the primary applications of 6-Methoxy-1H-indole-3-carbaldehyde is in the synthesis of indole-based compounds. The presence of the methoxy group at the sixth position and the aldehyde functional group allows for selective derivatization and further modification of the molecule. This enables chemists to create complex organic molecules with specific biological activities.Additionally, 6-Methoxy-1H-indole-3-carbaldehyde is often employed as a key intermediate in the preparation of natural products and bioactive compounds. Its structural features make it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and functional materials. Researchers can exploit its reactivity to introduce desired functional groups and tailor the properties of the final products.Moreover, this compound serves as a valuable tool in academic research, where its unique reactivity and structural motifs contribute to the development of new synthetic methodologies and strategies. Chemists can leverage its versatile nature to explore new reaction pathways and enhance the efficiency of chemical transformations.In summary, 6-Methoxy-1H-indole-3-carbaldehyde is a valuable chemical building block with diverse applications in chemical synthesis. Its structural features make it a versatile tool for creating complex organic molecules and exploring new avenues in drug discovery, material science, and academic research.