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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)-

1H-Imidazo[4,5-b]pyridine, 2-chloro-

Clc1nc2c([nH]1)cccn2 Request for Quotation
Chemical Name: 1H-Imidazo[4,5-b]pyridine, 2-chloro-
CAS Number: 104685-82-7
Product Number: AG007XP5(AGN-PC-0020UT)
Synonyms:
MDL No:
Molecular Formula: C6H4ClN3
Molecular Weight: 153.5691

Identification/Properties

Computed Properties
Molecular Weight:
153.569g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
153.009g/mol
Monoisotopic Mass:
153.009g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-1H-imidazo[4,5-b]pyridine, commonly referred to as $name$, is a versatile chemical compound with significant applications in modern chemical synthesis. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural features and reactivity.In chemical synthesis, 2-Chloro-1H-imidazo[4,5-b]pyridine is often employed as a valuable intermediate in the construction of heterocyclic compounds. Its presence in a molecule can impart specific pharmacological properties or enhance the biological activity of the final product. Additionally, this compound can participate in diverse synthetic transformations, such as cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed processes, making it a valuable tool for organic chemists.Moreover, the functional groups present in 2-Chloro-1H-imidazo[4,5-b]pyridine enable further modifications and derivatizations, allowing chemists to tailor the compound for specific applications. By judiciously incorporating this building block into synthetic pathways, researchers can access structurally complex molecules efficiently and explore new avenues in drug discovery and materials science.