2-(4-Fluorophenyl)propan-2-amine hydrochloride


Chemical Name: 2-(4-Fluorophenyl)propan-2-amine hydrochloride
CAS Number: 1216563-60-8
Product Number: AG00A0J5(AGN-PC-0WNNGQ)
Synonyms:
MDL No: MFCD11855812
Molecular Formula: C9H13ClFN
Molecular Weight: 189.6576

Identification/Properties


Computed Properties
Molecular Weight:
189.658g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
189.072g/mol
Monoisotopic Mass:
189.072g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
126
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:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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



2-(4-fluorophenyl)propan-2-amine hydrochloride is a versatile compound widely utilized in chemical synthesis for various applications. As a key intermediate in organic chemistry, this compound serves as a crucial building block in the creation of complex molecules and pharmaceuticals. Its unique structure, featuring a fluorine-substituted phenyl group and a secondary amine, offers a wide range of reactivity and functionalization possibilities in synthesis processes.In the realm of drug discovery and development, 2-(4-fluorophenyl)propan-2-amine hydrochloride plays a vital role in the synthesis of novel pharmacological agents and therapeutic compounds. The presence of the fluorophenyl moiety enhances the compound's biological activity and can be tailored to target specific biological pathways, making it an essential component in medicinal chemistry research.Furthermore, this compound's versatility extends to the synthesis of advanced materials, such as polymers, catalysts, and specialty chemicals. Its precise chemical structure and reactivity enable scientists to design and construct intricate molecular architectures with tailored properties for various industrial applications.Overall, 2-(4-fluorophenyl)propan-2-amine hydrochloride's significance in chemical synthesis lies in its ability to serve as a fundamental building block for the creation of diverse compounds with specific functions and applications in drug development, materials science, and other fields of research.