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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-Propanamine, 3-(3-methylphenoxy)-

NCCCOc1cccc(c1)C Request for Quotation
Chemical Name: 1-Propanamine, 3-(3-methylphenoxy)-
CAS Number: 26646-51-5
Product Number: AG007KXL(AGN-PC-0LWTPI)
Synonyms:
MDL No: MFCD08271804
Molecular Formula: C10H15NO
Molecular Weight: 165.2322

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(m-Tolyloxy)propan-1-amine is a key intermediate in organic synthesis, widely used as a versatile building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential component in the synthesis of complex organic molecules.In chemical synthesis, 3-(m-Tolyloxy)propan-1-amine serves as a valuable starting material for the construction of diverse scaffolds through functionalization reactions. Its amine functional group allows for facile derivatization, enabling the introduction of different substituents to tailor the properties of the final compound. Additionally, the presence of the tolyloxy moiety offers opportunities for selective transformations, such as aromatic substitutions and cross-coupling reactions.Moreover, the three-carbon chain in 3-(m-Tolyloxy)propan-1-amine provides a suitable backbone for the incorporation of various functional groups, enhancing the structural diversity of the synthesized compounds. This intermediate's compatibility with common synthetic methods and its versatility in forming C-C and C-N bonds make it a valuable reagent in the synthesis of biologically active molecules and functional materials.