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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, 4,6-dimethoxy-

COc1cc(OC)c2c(c1)[nH]cc2 Request for Quotation
Chemical Name: 1H-Indole, 4,6-dimethoxy-
CAS Number: 23659-87-2
Product Number: AG002O1L(AGN-PC-0JWNZ6)
Synonyms:
MDL No:
Molecular Formula: C10H11NO2
Molecular Weight: 177.1998

Identification/Properties

Properties
MP:
122-124 °C
BP:
343.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
177.203g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
177.079g/mol
Monoisotopic Mass:
177.079g/mol
Topological Polar Surface Area:
34.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,6-Dimethoxyindole is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In the realm of organic chemistry, this indole derivative serves as a valuable building block in the synthesis of various complex molecules. Its application as a key intermediate in the creation of novel pharmaceuticals, agrochemicals, and natural products showcases its significance in drug discovery and development.One notable application of 4,6-Dimethoxyindole is in the construction of heterocyclic compounds, where its indole moiety plays a crucial role in forming diverse ring structures. Through various synthetic methodologies such as condensation reactions, oxidation processes, and cyclization reactions, this compound can be manipulated to introduce specific functional groups, enabling the generation of structurally intricate molecules with desired biological activities.Moreover, the presence of methoxy groups at specific positions on the indole ring imparts distinct electronic properties to 4,6-Dimethoxyindole, allowing for tailored reactivity in chemical transformations. This characteristic feature enables chemists to fine-tune the regioselectivity and stereoselectivity of reactions involving this compound, facilitating the synthesis of stereochemically complex compounds efficiently.Overall, the versatile nature of 4,6-Dimethoxyindole in chemical synthesis offers a wide range of possibilities for producing valuable compounds with diverse applications in medicinal chemistry, agrochemistry, and materials science. Its strategic role as a synthetic building block underscores its importance in the pursuit of developing new and innovative chemical entities for various industrial sectors.