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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-Propanamine, 3,3'-(hydroxynitrosohydrazono)bis-

NCCCN(N(N=O)O)CCCN Request for Quotation
Chemical Name: 1-Propanamine, 3,3'-(hydroxynitrosohydrazono)bis-
CAS Number: 146724-95-0
Product Number: AG001E9U(AGN-PC-0JNEL7)
Synonyms:
MDL No: MFCD00797678
Molecular Formula: C6H17N5O2
Molecular Weight: 191.2315

Identification/Properties

Computed Properties
Molecular Weight:
191.235g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
7
Exact Mass:
191.138g/mol
Monoisotopic Mass:
191.138g/mol
Topological Polar Surface Area:
117A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
144
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,3′-(2-Hydroxy-2-nitrosohydrazinylidene)bis[1-propanamine], commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable reagent in various organic reactions.In chemical synthesis, $name$ is often employed as a catalyst or a reagent in the formation of complex molecules. Its ability to participate in multiple reactions simultaneously makes it a powerful tool in the hands of synthetic chemists. One key application of $name$ is in the formation of heterocyclic compounds, where it serves as a key building block in the synthesis of diverse chemical structures.Moreover, $name$ is known for its ability to facilitate redox reactions, making it an essential component in the construction of intricate organic frameworks. Its versatile nature allows for the selective modification of functional groups, enabling chemists to design and synthesize novel compounds with specific properties.Overall, the use of 3,3′-(2-Hydroxy-2-nitrosohydrazinylidene)bis[1-propanamine] in chemical synthesis showcases its importance as a valuable reagent in the development of new molecules with potential applications in medicine, materials science, and beyond.