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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)-

Quinoline, 1-acetyl-6-bromo-1,2,3,4-tetrahydro-

Brc1ccc2c(c1)CCCN2C(=O)C Request for Quotation
Chemical Name: Quinoline, 1-acetyl-6-bromo-1,2,3,4-tetrahydro-
CAS Number: 22190-40-5
Product Number: AG003DWO(AGN-PC-0JLY4G)
Synonyms:
MDL No: MFCD05664819
Molecular Formula: C11H12BrNO
Molecular Weight: 254.1231

Identification/Properties

Properties
BP:
436.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
254.127g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
253.01g/mol
Monoisotopic Mass:
253.01g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-Acetyl-6-bromo-1,2,3,4-tetrahydroquinoline is a versatile compound widely used in chemical synthesis as a key building block for the production of various important molecules. Its unique structure and reactivity make it an essential intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic materials.In chemical synthesis, 1-Acetyl-6-bromo-1,2,3,4-tetrahydroquinoline serves as a valuable starting material for the preparation of heterocyclic compounds, which are prevalent in medicinal chemistry. Its bromine substituent can undergo a variety of transformations, such as nucleophilic substitutions, palladium-catalyzed cross-coupling reactions, and metal-catalyzed coupling reactions, allowing for the introduction of diverse functional groups. The acetyl group provides a handle for further modification, enabling the fine-tuning of the compound's properties.Furthermore, the tetrahydroquinoline framework of this molecule imparts structural diversity and complexity to the synthesized products, making it an attractive scaffold for drug discovery and development. By utilizing 1-Acetyl-6-bromo-1,2,3,4-tetrahydroquinoline in chemical synthesis, researchers can access novel compounds with enhanced biological activities and improved pharmacokinetic profiles, thus accelerating the discovery of new therapeutics and agrochemicals.