1. Home
  2. 3,6-dibromoimidazo[1,2-a]pyridine

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

3,6-dibromoimidazo[1,2-a]pyridine

Brc1ccc2n(c1)c(Br)cn2 Request for Quotation
Chemical Name: 3,6-dibromoimidazo[1,2-a]pyridine
CAS Number: 1065074-14-7
Product Number: AG003IQA(AGN-PC-07XU2R)
Synonyms:
MDL No: MFCD11504879
Molecular Formula: C7H4Br2N2
Molecular Weight: 275.9281

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
275.931g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
275.872g/mol
Monoisotopic Mass:
273.874g/mol
Topological Polar Surface Area:
17.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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

Request for Quotation

Customer Feedback

Chemical Structure


3,6-Dibromoimidazo[1,2-a]pyridine is a versatile building block commonly used in chemical synthesis for the creation of novel compounds. This heterocyclic molecule plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science due to its unique structural properties and reactivity. In organic synthesis, it serves as a key intermediate in the production of various biologically active compounds and serves as a valuable precursor for functional group transformations. Additionally, 3,6-Dibromoimidazo[1,2-a]pyridine is often employed in the development of complex chemical structures with diverse applications in medicinal chemistry and materials research. Its ability to undergo a range of versatile reactions makes it an essential component in the toolbox of synthetic chemists aiming to access new molecules with potential therapeutic or material properties.