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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, 7-bromo-4-methoxy-

COc1ccc(c2c1cc[nH]2)Br Request for Quotation
Chemical Name: 1H-Indole, 7-bromo-4-methoxy-
CAS Number: 81224-16-0
Product Number: AG005F3K(AGN-PC-0KYR87)
Synonyms:
MDL No:
Molecular Formula: C9H8BrNO
Molecular Weight: 226.0699

Identification/Properties

Properties
BP:
356.5 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Bromo-4-methoxy-1H-indole is a versatile chemical compound widely used in chemical synthesis due to its unique properties and reactivity. With its bromine and methoxy functional groups, this compound serves as a valuable building block in the preparation of various advanced organic molecules. In chemical synthesis, 7-Bromo-4-methoxy-1H-indole can participate in a variety of reactions such as nucleophilic substitutions, cross-coupling reactions, and heterocyclic transformations. Its bromine atom can serve as a reactive site for further derivatization, allowing for the introduction of various functional groups to tailor the final compound's properties.This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its indole core imparts biological activity to the molecules it is incorporated into, making it a key component in drug discovery and development. Additionally, its methoxy group can influence the compound's solubility and lipophilicity, further expanding its applications in medicinal chemistry.Overall, 7-Bromo-4-methoxy-1H-indole plays a crucial role in modern organic synthesis, enabling chemists to access a wide range of complex molecules with diverse functionalities for various applications.