1. Home
  2. 6-Bromo-3-Iodo quinoline

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-3-Iodo quinoline

Brc1ccc2c(c1)cc(cn2)I Request for Quotation
Chemical Name: 6-Bromo-3-Iodo quinoline
CAS Number: 1416440-23-7
Product Number: AG001GTB(AGN-PC-0WAIYE)
Synonyms:
MDL No:
Molecular Formula: C9H5BrIN
Molecular Weight: 333.9512

Identification/Properties

Computed Properties
Molecular Weight:
333.954g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
332.865g/mol
Monoisotopic Mass:
332.865g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


6-Bromo-3-iodoquinoline, a versatile chemical compound, finds wide application in the field of chemical synthesis. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 6-Bromo-3-iodoquinoline exhibits unique reactivity and functional group tolerance, making it an excellent intermediate for the creation of complex molecular structures. Its strategic positioning of bromine and iodine atoms enables facile derivatization and manipulation, allowing for the introduction of specific functional groups at precise locations within a molecule.Moreover, the presence of both bromine and iodine moieties in 6-Bromo-3-iodoquinoline imparts desirable properties to the resulting products, such as enhanced bioactivity and chemical stability. This compound acts as a key component in the construction of molecular scaffolds that are crucial for the development of novel drug candidates, agrochemicals with improved efficacy, and advanced materials with tailored properties.Overall, 6-Bromo-3-iodoquinoline plays a vital role in modern chemical synthesis by acting as a versatile reagent that enables the efficient and selective formation of complex molecules with diverse applications in the pharmaceutical, agricultural, and materials industries.