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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)-

1-Pentanamine, N-nitroso-N-pentyl-

CCCCCN(N=O)CCCCC Request for Quotation
Chemical Name: 1-Pentanamine, N-nitroso-N-pentyl-
CAS Number: 13256-06-9
Product Number: AG0010UE(AGN-PC-0JNQRO)
Synonyms:
MDL No:
Molecular Formula: C10H22N2O
Molecular Weight: 186.2945

Identification/Properties

Computed Properties
Molecular Weight:
186.299g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
8
Exact Mass:
186.173g/mol
Monoisotopic Mass:
186.173g/mol
Topological Polar Surface Area:
32.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
108
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


N,N-Diamylnitrosamine is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. As a nitrosamine derivative, it serves as a valuable building block in the creation of various organic compounds due to its ability to undergo diverse chemical transformations. In organic synthesis, N,N-Diamylnitrosamine is often employed as a precursor for the preparation of complex nitrogen-containing molecules and heterocyclic compounds. Its versatile nature allows for the efficient incorporation of functional groups and structural motifs into target molecules, making it an essential reagent for the construction of diverse chemical structures. Additionally, N,N-Diamylnitrosamine plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science, where its synthetic utility enables the design and production of novel compounds with specific properties and functionalities. By leveraging the reactivity and versatility of N,N-Diamylnitrosamine in chemical synthesis, researchers and chemists can explore new avenues for the creation of innovative materials and compounds with potential applications across various industries.