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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)-

Piperazine, 1-[(5-chloro-1H-benzimidazol-2-yl)carbonyl]-4-methyl-,(2Z)-2-butenedioate (1:1)

CN1CCN(CC1)C(=O)c1nc2c([nH]1)ccc(c2)Cl.OC(=O)/C=CC(=O)O Request for Quotation
Chemical Name: Piperazine, 1-[(5-chloro-1H-benzimidazol-2-yl)carbonyl]-4-methyl-,(2Z)-2-butenedioate (1:1)
CAS Number: 869497-75-6
Product Number: AG004O7A(AGN-PC-0V9EJC)
Synonyms:
MDL No: MFCD09878266
Molecular Formula: C17H19ClN4O5
Molecular Weight: 394.8096

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
394.812g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
394.104g/mol
Monoisotopic Mass:
394.104g/mol
Topological Polar Surface Area:
127A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
465
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-[(5-Chloro-1H-benzimidazol-2-yl)carbonyl]-4-methylpiperazine maleate is a versatile compound utilized in chemical synthesis for its unique properties and reactivity. This molecule serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its functional groups and structural characteristics. In chemical synthesis, this maleate derivative acts as a valuable intermediate in the formation of complex organic compounds, enabling the development of novel substances with potential applications in medicinal chemistry and beyond. Its strategic placement of functional groups makes it an essential component in the preparation of diverse molecular structures, facilitating the exploration of new pathways and methodologies in the synthesis of biologically active compounds.