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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-Chloro-8-fluoroimidazo[1,2-a]pyridine

Clc1cc(F)c2n(c1)ccn2 Request for Quotation
Chemical Name: 6-Chloro-8-fluoroimidazo[1,2-a]pyridine
CAS Number: 1033202-10-6
Product Number: AG007GYS(AGN-PC-0WNPYJ)
Synonyms:
MDL No:
Molecular Formula: C7H4ClFN2
Molecular Weight: 170.5715

Identification/Properties

Computed Properties
Molecular Weight:
170.571g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
170.005g/mol
Monoisotopic Mass:
170.005g/mol
Topological Polar Surface Area:
17.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-8-fluoroimidazo[1,2-a]pyridine is a versatile compound commonly used in chemical synthesis for its unique structural properties and reactivity. It serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its heterocyclic nature, 6-Chloro-8-fluoroimidazo[1,2-a]pyridine can participate in a wide range of organic reactions, including nucleophilic substitutions, cross-coupling reactions, and cycloadditions. Its presence in the molecular structure of the final product can impart desirable biological activities or physical properties, making it an essential component in the synthesis of diverse functional molecules.