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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-bromo-7-chloro-2,3-dihydro-

Brc1cc(Cl)c2c(c1)CCN2 Request for Quotation
Chemical Name: 1H-Indole, 5-bromo-7-chloro-2,3-dihydro-
CAS Number: 221024-31-3
Product Number: AG00BHQS(AGN-PC-0165A4)
Synonyms:
MDL No:
Molecular Formula: C8H7BrClN
Molecular Weight: 232.50488

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-7-chloroindoline is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly utilized as a building block in the production of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it an essential component in the creation of complex organic molecules. Additionally, 5-Bromo-7-chloroindoline serves as a key intermediate in the synthesis of heterocyclic compounds, which are widely used in the development of new drugs and materials. Its compatibility with a range of chemical reactions makes it a valuable tool for chemists seeking to create novel compounds with diverse applications in the field of chemistry.