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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)-

Imidazo[1,2-a]pyridine, 6-chloro-

Clc1ccc2n(c1)ccn2 Request for Quotation
Chemical Name: Imidazo[1,2-a]pyridine, 6-chloro-
CAS Number: 6188-25-6
Product Number: AG003N6H(AGN-PC-0KKQ5Q)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2
Molecular Weight: 152.5810

Identification/Properties

Properties
MP:
85-87 °C
BP:
132 °C at 1.5 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
152.581g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
152.014g/mol
Monoisotopic Mass:
152.014g/mol
Topological Polar Surface Area:
17.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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


6-Chloroimidazo[1,2-a]pyridine is a versatile building block in chemical synthesis and is commonly used in the pharmaceutical industry and academic research. This compound serves as a key intermediate in the preparation of various biologically active molecules, including pharmaceuticals and agrochemicals.In organic synthesis, 6-Chloroimidazo[1,2-a]pyridine can undergo a variety of reactions such as nucleophilic substitution, palladium-catalyzed coupling, and metal-catalyzed cross-coupling reactions. These transformations enable the modification of the molecular structure to introduce specific functional groups, which is essential for the development of new compounds with desired properties.One of the main applications of 6-Chloroimidazo[1,2-a]pyridine is in the synthesis of heterocyclic compounds, which are commonly found in various pharmaceutical products due to their diverse biological activities. By incorporating this building block into the molecular structure, chemists can access a wide range of chemical space and potentially discover novel drug candidates with improved pharmacological profiles.Overall, the versatility and reactivity of 6-Chloroimidazo[1,2-a]pyridine make it a valuable tool for chemists involved in drug discovery, medicinal chemistry, and chemical research. Its ability to participate in different types of chemical reactions highlights its importance in the development of complex molecules for various applications.