3-amino-3-phenylpropan-1-ol


Chemical Name: 3-amino-3-phenylpropan-1-ol
CAS Number: 14593-04-5
Product Number: AG001DIU(AGN-PC-0JMZD2)
Synonyms:
MDL No: MFCD00801124
Molecular Formula: C9H13NO
Molecular Weight: 151.2056

Identification/Properties


Properties
MP:
70-77 °C
BP:
293°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
1.4755 (estimate)
Computed Properties
Molecular Weight:
151.209g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
151.1g/mol
Monoisotopic Mass:
151.1g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
99.7
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



3-Amino-3-Phenyl-1-Propanol is a versatile compound widely utilized in chemical synthesis for its unique properties and applications. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. Its distinctive structure allows for the introduction of functional groups at different positions, enabling the creation of complex molecules with specific properties.In organic synthesis, 3-Amino-3-Phenyl-1-Propanol serves as an important intermediate in the production of chiral compounds, which are crucial in the pharmaceutical industry for the development of enantiopure drugs. Its chiral nature makes it a valuable starting material for the synthesis of amino alcohols, amino acids, and other bioactive molecules.Furthermore, 3-Amino-3-Phenyl-1-Propanol is employed in the preparation of ligands for catalysis, where its amino and hydroxyl groups can coordinate with metal ions to form stable complexes. These complexes play a vital role in various catalytic processes, including asymmetric hydrogenation, hydroformylation, and cross-coupling reactions.Additionally, this compound finds application in the synthesis of surfactants, polymers, and specialty chemicals due to its ability to modify the surface properties of materials and enhance their performance. Its versatile chemistry and reactivity make it a valuable tool for organic chemists seeking to create new molecules with tailored properties for a wide range of applications.