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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-methylimidazo[1,2-a]pyridine;hydrochloride

Cc1cc2nccn2cc1Br.Cl Request for Quotation
Chemical Name: 6-bromo-7-methylimidazo[1,2-a]pyridine;hydrochloride
CAS Number: 957035-22-2
Product Number: AG003N4M(AGN-PC-0712PT)
Synonyms:
MDL No:
Molecular Formula: C8H8BrClN2
Molecular Weight: 247.5195

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
247.52g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
245.956g/mol
Monoisotopic Mass:
245.956g/mol
Topological Polar Surface Area:
17.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
151
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-7-methylimidazo[1,2-a]pyridine hydrochloride is a versatile chemical compound commonly used in organic synthesis. It serves as an important building block in the creation of pharmaceuticals, agrochemicals, and fine chemicals. By incorporating this compound into chemical reactions, chemists can introduce a bromine atom and a methyl group into a heterocyclic structure, thereby modulating the physicochemical properties and biological activities of the resulting products. Its unique structure makes it a valuable tool for medicinal chemists seeking to design novel drug candidates with improved pharmacological properties. Additionally, its reactivity and compatibility with various functional groups make it an ideal reagent for the efficient synthesis of complex molecules in drug discovery and development processes.