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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)-

6-Bromo-2,3-dihydro-1H-indole hydrochloride

Brc1ccc2c(c1)NCC2.Cl Request for Quotation
Chemical Name: 6-Bromo-2,3-dihydro-1H-indole hydrochloride
CAS Number: 1187933-30-7
Product Number: AG009409(AGN-PC-07HAZE)
Synonyms:
MDL No:
Molecular Formula: C8H9BrClN
Molecular Weight: 234.5208

Identification/Properties

Computed Properties
Molecular Weight:
234.521g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
232.961g/mol
Monoisotopic Mass:
232.961g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
126
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromoindoline hydrochloride is a versatile organic compound frequently employed in chemical synthesis as a key building block. This compound serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique reactivity allows for selective functionalization, enabling the construction of complex molecular structures with high efficiency. In particular, 6-Bromoindoline hydrochloride is utilized in the synthesis of indole derivatives, which are important scaffolds in medicinal chemistry. Its strategic incorporation into synthetic routes facilitates the introduction of diverse functional groups and enables the rapid assembly of structurally diverse compounds. Additionally, the presence of the bromo group renders 6-Bromoindoline hydrochloride amenable to cross-coupling reactions, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Overall, this compound plays a crucial role in the synthesis of bioactive molecules and materials with potential applications in various fields.