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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)-

7-chloropyrido[3,4-b]pyrazine

Clc1ncc2c(c1)nccn2 Request for Quotation
Chemical Name: 7-chloropyrido[3,4-b]pyrazine
CAS Number: 93049-39-9
Product Number: AG006J5J(AGN-PC-0713G2)
Synonyms:
MDL No:
Molecular Formula: C7H4ClN3
Molecular Weight: 165.5798

Identification/Properties

Properties
BP:
314.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
165.58g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
165.009g/mol
Monoisotopic Mass:
165.009g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
142
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


7-Chloropyrido[3,4-b]pyrazine is a versatile building block used in chemical synthesis for the creation of a wide range of functional molecules. This compound is often employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and various fine chemicals. Its unique structure and reactivity make it valuable in the development of new compounds with potential applications in drug discovery and material science.In organic synthesis, 7-Chloropyrido[3,4-b]pyrazine can be utilized for the construction of heterocyclic compounds through various transformations such as substitution reactions, cross-coupling reactions, and cycloadditions. Its chloro group allows for further functionalization, enabling the introduction of various substituents that can modulate the properties of the final products. Additionally, its pyridine and pyrazine units provide opportunities for diversification and structural modification, making it an essential building block for scaffold-based synthesis strategies.Overall, the versatile nature of 7-Chloropyrido[3,4-b]pyrazine makes it a valuable tool in chemical synthesis for the creation of novel compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.