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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, 5-(1-methylethyl)-

CC(c1ccc2c(c1)cc[nH]2)C Request for Quotation
Chemical Name: 1H-Indole, 5-(1-methylethyl)-
CAS Number: 97820-51-4
Product Number: AG005XPV(AGN-PC-0N6KEI)
Synonyms:
MDL No:
Molecular Formula: C11H13N
Molecular Weight: 159.2276

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


5-(1-Methylethyl)-1H-indole, also known as isopropylindole, is a versatile chemical compound commonly used in organic synthesis. This unique indole derivative serves as a valuable building block in a variety of chemical reactions, enabling the creation of complex molecular structures with diverse functionalities. In chemical synthesis, 5-(1-Methylethyl)-1H-indole can be employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials science. Its structural properties provide a platform for the introduction of different functional groups through various synthetic methodologies, allowing for the customization of molecular architectures for specific applications. Furthermore, the presence of the isopropyl group enhances the compound's reactivity and compatibility with a wide range of reactants, facilitating efficient synthetic routes and enabling the rapid formation of target molecules. From drug discovery to material design, the versatile nature of 5-(1-Methylethyl)-1H-indole makes it an indispensable tool in the toolkit of synthetic chemists seeking to develop novel compounds with tailored properties and functions.