1H-Pyrazole-1-propanamine


Chemical Name: 1H-Pyrazole-1-propanamine
CAS Number: 75653-86-0
Product Number: AG005IYB(AGN-PC-0LWA42)
Synonyms:
MDL No:
Molecular Formula: C6H11N3
Molecular Weight: 125.1716

Identification/Properties


Properties
BP:
225.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
125.175g/mol
XLogP3:
-1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
125.095g/mol
Monoisotopic Mass:
125.095g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
74.7
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



3-(1H-Pyrazol-1-yl)propan-1-amine, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a crucial building block in organic chemistry and finds various applications in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 3-(1H-Pyrazol-1-yl)propan-1-amine is commonly employed as a key intermediate for the synthesis of diverse heterocyclic compounds. Its unique structure containing a pyrazole ring and an amine group allows for the efficient construction of complex molecular structures. Additionally, the presence of the propyl chain provides flexibility for further functionalization, enabling the synthesis of a wide range of derivatives with tailored properties.One of the prominent applications of 3-(1H-Pyrazol-1-yl)propan-1-amine is in the development of novel pharmaceutical compounds. By incorporating this compound into molecular frameworks, chemists can explore its pharmacological potential and create new drug candidates with enhanced biological activities. Furthermore, its role in agrochemical synthesis contributes to the design of crop protection agents and plant growth regulators with improved efficacy and environmental safety.Moreover, the use of 3-(1H-Pyrazol-1-yl)propan-1-amine in materials science enables the creation of functional materials with desired properties. Its ability to act as a linker in coordination chemistry facilitates the construction of metal-organic frameworks, which exhibit diverse applications in gas storage, catalysis, and sensing technologies. Additionally, the incorporation of this compound into polymer backbones can lead to the development of advanced materials with tunable characteristics for various industrial applications.