1,4-Butanediamine, N,N'-di-2,3-butadienyl-, dihydrochloride


Chemical Name: 1,4-Butanediamine, N,N'-di-2,3-butadienyl-, dihydrochloride
CAS Number: 93565-01-6
Product Number: AG006208(AGN-PC-0W359K)
Synonyms:
MDL No:
Molecular Formula: C12H22Cl2N2
Molecular Weight: 265.2225

Identification/Properties


Properties
BP:
300.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Solubility:
H2O: soluble15mg/mL, clear
Computed Properties
Molecular Weight:
265.222g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
9
Exact Mass:
264.116g/mol
Monoisotopic Mass:
264.116g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
184
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:
3
Compound Is Canonicalized:
No

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a key building block in the creation of complex organic molecules, where its unique structure and reactivity play a crucial role in various reactions.In chemical synthesis, N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride acts as a valuable reagent for forming carbon-carbon bonds through cross-coupling reactions. Its butadiene moieties enable it to participate in diverse transformations, facilitating the construction of intricate molecular frameworks. Additionally, its diamine functionality imparts the ability to introduce nitrogen atoms into target molecules, allowing for the synthesis of nitrogen-containing compounds with enhanced properties.Furthermore, the dihydrochloride salt form of this compound provides ease of handling and improved solubility in various reaction solvents, enhancing its utility in synthetic procedures. Whether employed in the preparation of pharmaceutical intermediates, agrochemicals, or materials science applications, N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride proves to be an indispensable tool for chemists seeking to access structurally diverse and functionally rich compounds.