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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-7-chloro-1-indanone

O=C1CCc2c1c(Cl)c(cc2)Br Request for Quotation
Chemical Name: 6-Bromo-7-chloro-1-indanone
CAS Number: 1337850-20-0
Product Number: AG00HSZP(AGN-PC-0WR40S)
Synonyms:
MDL No: MFCD20462304
Molecular Formula: C9H6BrClO
Molecular Weight: 245.5003

Identification/Properties

Computed Properties
Molecular Weight:
245.5g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
243.929g/mol
Monoisotopic Mass:
243.929g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
207
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

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


6-Bromo-7-chloro-2,3-dihydro-1H-inden-1-one is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the synthesis of various organic molecules, especially pharmaceuticals and agrochemicals. Its strategic placement of bromine and chlorine atoms provides opportunities for further functionalization and diversification of chemical structures. In particular, the presence of the bromo and chloro substituents allows for selective cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings, enabling the formation of complex molecular frameworks. Additionally, the indenone core of this compound offers opportunities for the generation of diverse heterocyclic systems through cyclization reactions. The resulting compounds derived from 6-Bromo-7-chloro-2,3-dihydro-1H-inden-1-one exhibit a range of biological activities and have found applications in drug discovery and development processes. Overall, this compound plays a crucial role in the synthesis of advanced organic molecules with potential therapeutic or agricultural significance.