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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-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine

Clc1ccc2c(n1)NCCN2 Request for Quotation
Chemical Name: 6-chloro-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine
CAS Number: 1210129-64-8
Product Number: AG008SWO(AGN-PC-07HB47)
Synonyms:
MDL No:
Molecular Formula: C7H8ClN3
Molecular Weight: 169.6115

Identification/Properties

Computed Properties
Molecular Weight:
169.612g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
169.041g/mol
Monoisotopic Mass:
169.041g/mol
Topological Polar Surface Area:
37A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine is a versatile compound widely utilized in chemical synthesis as a key building block. Due to its unique structure and reactivity, this compound serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. In organic synthesis, 6-Chloro-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine can participate in a range of transformations, such as nucleophilic substitution, cross-coupling reactions, and cyclization processes, enabling the efficient construction of complex molecular structures. Its presence in the synthesis of heterocyclic compounds and biologically active molecules highlights its significance in the development of novel chemical entities with potential applications in drug discovery and material science. Additionally, the ability of 6-Chloro-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine to undergo diverse functionalization reactions further enhances its utility as a versatile synthetic building block, allowing for the creation of tailored compounds with specific properties and functions.