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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,3-diphenyl-2-aminopropane

NC(Cc1ccccc1)Cc1ccccc1 Request for Quotation
Chemical Name: 1,3-diphenyl-2-aminopropane
CAS Number: 4275-43-8
Product Number: AG00CNE7(AGN-00CN8N)
Synonyms:
MDL No:
Molecular Formula: C15H17N
Molecular Weight: 211.3022

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
211.308g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
211.136g/mol
Monoisotopic Mass:
211.136g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
158
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,3-Diphenylpropan-2-amine, also known as DPPA, is a versatile compound widely utilized in chemical synthesis for various applications. In organic chemistry, DPPA serves as a key intermediate in the synthesis of a range of pharmaceuticals, agrochemicals, and fine chemicals. Its amine functional group allows for selective reactivity in numerous transformations, making it an essential building block in the production of diverse chemical compounds.One of the primary applications of 1,3-Diphenylpropan-2-amine is as a precursor in reductive amination reactions. By reacting DPPA with various carbonyl compounds and reducing agents, chemists can efficiently introduce the amine moiety into the molecules, enabling the synthesis of complex nitrogen-containing organic compounds.Additionally, 1,3-Diphenylpropan-2-amine can be employed in the preparation of heterocyclic compounds, such as imines and enamines, through condensation reactions. These heterocycles play crucial roles in medicinal chemistry and material science, further highlighting the significance of DPPA in chemical synthesis.Overall, the strategic utilization of 1,3-Diphenylpropan-2-amine in chemical synthesis enables the efficient construction of diverse molecular scaffolds, facilitating the development of novel compounds with promising applications across various industries.