1H-Pyrazol-3-amine, 5-propyl-


Chemical Name: 1H-Pyrazol-3-amine, 5-propyl-
CAS Number: 126748-58-1
Product Number: AG000T6C(AGN-PC-03N23H)
Synonyms:
MDL No: MFCD08061095
Molecular Formula: C6H11N3
Molecular Weight: 125.1716

Identification/Properties


Properties
MP:
37-40°C
BP:
316.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
125.175g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
125.095g/mol
Monoisotopic Mass:
125.095g/mol
Topological Polar Surface Area:
54.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
84.4
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

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NMR Spectrum


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Chemical Structure



5-Propyl-1H-pyrazol-3-amine is a versatile chemical compound commonly used in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the creation of various organic molecules and pharmaceuticals. With its distinct molecular structure, 5-Propyl-1H-pyrazol-3-amine can participate in a variety of reactions such as substitution, oxidation, and reduction.One of the primary applications of 5-Propyl-1H-pyrazol-3-amine is in the pharmaceutical industry, where it is utilized in the synthesis of potential drug candidates. Its presence in the molecular structure of certain compounds can confer specific biological activities, making it a valuable tool in drug discovery and development. Additionally, this compound is employed in academic research settings for the preparation of novel molecules with diverse functions.In organic synthesis, 5-Propyl-1H-pyrazol-3-amine is often employed as a precursor for modifying existing compounds or generating new chemical entities. Its ability to undergo various transformations under appropriate reaction conditions makes it a sought-after reagent in the synthesis of complex organic molecules. Chemists utilize this compound to introduce specific functional groups into target molecules, enabling the generation of tailored compounds for specific applications.Overall, the versatility and reactivity of 5-Propyl-1H-pyrazol-3-amine make it an indispensable tool in chemical synthesis, enabling the construction of diverse molecules with potential applications in pharmaceuticals, materials science, and other research fields.