1. Home
  2. 5-bromoimidazo[1,2-a]pyridine-2-carboxylic acid

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)-

5-bromoimidazo[1,2-a]pyridine-2-carboxylic acid

OC(=O)c1cn2c(n1)cccc2Br Request for Quotation
Chemical Name: 5-bromoimidazo[1,2-a]pyridine-2-carboxylic acid
CAS Number: 1026201-52-4
Product Number: AG0007YE(AGN-PC-0CTWGS)
Synonyms:
MDL No:
Molecular Formula: C8H5BrN2O2
Molecular Weight: 241.0415

Identification/Properties

Computed Properties
Molecular Weight:
241.044g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
239.953g/mol
Monoisotopic Mass:
239.953g/mol
Topological Polar Surface Area:
54.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
224
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-Bromoimidazo[1,2-a]pyridine-2-carboxylic acid, often referred to as $name$, is a versatile chemical compound widely utilized in chemical synthesis processes. This compound plays a crucial role in the development and production of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity. In chemical synthesis, $name$ serves as a key building block, enabling the formation of complex structures through functional group transformations and molecular modifications. Its presence facilitates the creation of diverse molecules with specific biological activities or material properties, making it an invaluable tool in the field of organic chemistry. Additionally, the incorporation of $name$ in multi-step synthesis processes allows for the efficient production of desired compounds with high purity and yield, contributing to advancements in drug discovery, materials science, and other areas of chemical research.