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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-(3-bromoquinolin-6-yl)ethanone

Brc1cnc2c(c1)cc(cc2)C(=O)C Request for Quotation
Chemical Name: 1-(3-bromoquinolin-6-yl)ethanone
CAS Number: 1150618-23-7
Product Number: AG000FU5(AGN-PC-05VCE6)
Synonyms:
MDL No:
Molecular Formula: C11H8BrNO
Molecular Weight: 250.0913

Identification/Properties

Computed Properties
Molecular Weight:
250.095g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
248.979g/mol
Monoisotopic Mass:
248.979g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(3-Bromoquinolin-6-yl)ethanone is a versatile compound that finds wide application in chemical synthesis processes. This compound functions as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable building block in organic synthesis, allowing for the creation of complex molecules with specific functional groups and properties. In particular, 1-(3-Bromoquinolin-6-yl)ethanone is employed in the synthesis of heterocyclic compounds, which are prevalent in many biologically active molecules. Additionally, this compound can be utilized in the development of novel materials and catalysts, showcasing its utility across different fields of chemistry. With its diverse applications and significant role in chemical synthesis, 1-(3-Bromoquinolin-6-yl)ethanone stands as a crucial component for researchers and professionals striving to innovate and advance in the realm of organic chemistry.