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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)-

Benzenamine, 4,4'-[1,5-pentanediylbis(oxy)]bis-

Nc1ccc(cc1)OCCCCCOc1ccc(cc1)N Request for Quotation
Chemical Name: Benzenamine, 4,4'-[1,5-pentanediylbis(oxy)]bis-
CAS Number: 2391-56-2
Product Number: AG003DPR(AGN-PC-0JKBLL)
Synonyms:
MDL No:
Molecular Formula: C17H22N2O2
Molecular Weight: 286.3688

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
286.375g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
286.168g/mol
Monoisotopic Mass:
286.168g/mol
Topological Polar Surface Area:
70.5A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
234
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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,5-Bis(4-aminophenoxy)pentane, commonly referred to as $name$, is a multifunctional compound that finds wide applications in various chemical synthesis processes. This unique molecule serves as a valuable building block in the creation of advanced materials, pharmaceuticals, and specialty chemicals. Due to its symmetric structure and versatile reactivity, $name$ is particularly favored in organic synthesis for the formation of complex molecular structures.In chemical synthesis, 1,5-Bis(4-aminophenoxy)pentane is often utilized as a crosslinking agent in the production of polymers and resins. Its ability to link multiple polymer chains together through covalent bonds imparts enhanced mechanical properties, thermal stability, and chemical resistance to the resulting materials. Moreover, the presence of amino groups in $name$ further facilitates functionalization reactions, allowing for the incorporation of specific properties or functionalities into the polymeric matrix.Additionally, 1,5-Bis(4-aminophenoxy)pentane serves as a key intermediate in the synthesis of biologically active compounds and pharmaceutical ingredients. By serving as a spacer molecule or a linker group, it enables the conjugation of bioactive molecules to enhance their pharmacokinetic profiles, targeting capabilities, or therapeutic effects. This application highlights the importance of $name$ in drug discovery and development processes, where precise control over molecular architecture is essential for optimizing drug efficacy and safety.Overall, the diverse applications of 1,5-Bis(4-aminophenoxy)pentane in chemical synthesis underscore its significance as a strategic tool for creating advanced materials and bioactive compounds with tailored properties and functionalities.