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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)-

Benzenepentanamine

NCCCCCc1ccccc1 Request for Quotation
Chemical Name: Benzenepentanamine
CAS Number: 17734-21-3
Product Number: AG00259G(AGN-PC-0JMR8F)
Synonyms:
MDL No:
Molecular Formula: C11H17N
Molecular Weight: 163.2594

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;
Form:
Liquid
Computed Properties
Molecular Weight:
163.264g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
5
Exact Mass:
163.136g/mol
Monoisotopic Mass:
163.136g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
95.2
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzenepentanamine, also known as dipentylamine, is widely utilized in various chemical synthesis applications. In organic chemistry, this compound serves as a versatile building block due to its aromatic and alkyl amine functional groups. One prominent application of Benzenepentanamine is in the preparation of novel functional materials. By incorporating this compound into the molecular structure of polymers, researchers can enhance specific properties such as thermal stability, mechanical strength, and chemical resistance. The presence of the benzene ring provides aromatic character, while the alkyl amine groups contribute to potential reactivity with other functional groups.Moreover, Benzenepentanamine's ability to undergo various substitution and addition reactions makes it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. It can be used to introduce specific functionalities or stereochemistry into complex molecules, facilitating the development of new drug candidates or crop protection agents.Furthermore, in the field of materials science, Benzenepentanamine can be employed in the fabrication of organic electronic devices such as OLEDs (organic light-emitting diodes) and OPVs (organic photovoltaics). The unique electronic properties of this compound make it a suitable candidate for enhancing charge transport and light absorption in these applications.Additionally, Benzenepentanamine finds utility in the synthesis of specialty chemicals, dyes, and surfactants. Its structural features offer opportunities for creating tailored molecules with desired properties for a range of industrial applications.Overall, the diverse reactivity and functionality of Benzenepentanamine make it a valuable component in chemical synthesis, driving innovation in various sectors of the chemical industry.