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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)-

1-(7-bromo-1H-indol-3-yl)ethanone

CC(=O)c1c[nH]c2c1cccc2Br Request for Quotation
Chemical Name: 1-(7-bromo-1H-indol-3-yl)ethanone
CAS Number: 944086-09-3
Product Number: AG00II52(AGN-PC-015DXA)
Synonyms:
MDL No:
Molecular Formula: C10H8BrNO
Molecular Weight: 238.0806

Identification/Properties

Computed Properties
Molecular Weight:
238.084g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
236.979g/mol
Monoisotopic Mass:
236.979g/mol
Topological Polar Surface Area:
32.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
219
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(7-Bromo-1H-indol-3-yl)ethanone is a versatile compound that finds application in various chemical synthesis processes. Its unique molecular structure contributes to its utility in the creation of diverse organic compounds.This compound serves as a valuable building block for the synthesis of pharmaceutical intermediates, agrochemicals, and functional materials. Its indole framework imparts specific reactivity properties, making it a valuable tool in the construction of complex molecular structures.In organic synthesis, 1-(7-Bromo-1H-indol-3-yl)ethanone can undergo various reactions such as nucleophilic addition, substitution, and condensation reactions to introduce different functional groups at the indole and ketone moieties. This flexibility allows for the tailored design and production of target molecules with specific properties for various applications in the fields of medicine, agriculture, and materials science.Furthermore, the presence of the bromine atom in the indole ring confers additional synthetic possibilities, enabling further derivatization and diversification of the compound. Overall, the application of 1-(7-Bromo-1H-indol-3-yl)ethanone in chemical synthesis showcases its importance as a foundational component in the creation of novel compounds with potential industrial and scientific relevance.