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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)-

Quinoxaline, 5-chloro-

Clc1cccc2c1nccn2 Request for Quotation
Chemical Name: Quinoxaline, 5-chloro-
CAS Number: 62163-09-1
Product Number: AG00EFUA(AGN-PC-0JTIAM)
Synonyms:
MDL No:
Molecular Formula: C8H5ClN2
Molecular Weight: 164.5917

Identification/Properties

Computed Properties
Molecular Weight:
164.592g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
164.014g/mol
Monoisotopic Mass:
164.014g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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

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Chemical Structure


5-Chloroquinoxaline, also known as 5-chloro-1,4-dihydroquinoxaline, is a versatile building block in organic synthesis due to its unique chemical properties. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and dyes. In chemical synthesis, 5-Chloroquinoxaline is frequently utilized as a precursor for the construction of biologically active compounds such as antimalarials, antibacterials, antifungals, and anticancer agents.One of the prominent applications of 5-Chloroquinoxaline is its role in the synthesis of heterocyclic compounds. By undergoing various functionalization reactions, this compound can be modified to introduce specific functional groups or structural motifs that are crucial for enhancing the biological activity of the final product. Additionally, 5-Chloroquinoxaline can participate in cross-coupling reactions, nucleophilic substitution, and oxidation reactions to enable the synthesis of complex organic molecules with diverse pharmacological properties.Furthermore, 5-Chloroquinoxaline exhibits excellent reactivity towards a wide range of nucleophiles and electrophiles, making it a valuable tool for chemists in designing and preparing novel chemical entities. Its ability to undergo regioselective and stereoselective transformations allows for the efficient construction of chiral molecules with high enantiomeric purity. Overall, the versatility of 5-Chloroquinoxaline in chemical synthesis makes it a valuable asset for researchers and synthetic chemists in the development of new therapeutic agents and functional materials.