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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-Propanol, 3-[bis(phenylmethyl)amino]-

OCCCN(Cc1ccccc1)Cc1ccccc1 Request for Quotation
Chemical Name: 1-Propanol, 3-[bis(phenylmethyl)amino]-
CAS Number: 3161-51-1
Product Number: AG003I7G(AGN-PC-0LB3T0)
Synonyms:
MDL No:
Molecular Formula: C17H21NO
Molecular Weight: 255.3547

Identification/Properties

Properties
BP:
389℃
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.562(lit.)
Computed Properties
Molecular Weight:
255.361g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
7
Exact Mass:
255.162g/mol
Monoisotopic Mass:
255.162g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
199
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Dibenzylamino)-1-propanol is a versatile chemical compound commonly used in chemical synthesis for a variety of applications. It serves as a valuable building block in the creation of a wide range of pharmaceuticals and specialty chemicals due to its unique structure and reactivity. This compound is particularly prized for its ability to act as a precursor in the synthesis of complex organic molecules, making it an essential tool for chemists working in the field of drug development and material science.In organic synthesis, 3-(Dibenzylamino)-1-propanol is often employed as a key intermediate in the formation of chiral compounds, which are molecules that exist in two non-superimposable mirror image forms known as enantiomers. These enantiomers can exhibit different biological activities and interactions, making them crucial in the design and production of pharmaceuticals with specific target effects. By utilizing 3-(Dibenzylamino)-1-propanol in chemical reactions, researchers can efficiently access enantiomerically pure compounds for further exploration and development.Furthermore, this compound can also serve as a useful starting material for the synthesis of various functionalized organic molecules, including amino alcohols and heterocyclic compounds. The presence of the dibenzylamino group in 3-(Dibenzylamino)-1-propanol allows for selective transformations and derivatizations, enabling chemists to introduce specific functionalities and structural motifs into their desired products. This versatility makes 3-(Dibenzylamino)-1-propanol a valuable asset in the toolkit of synthetic chemists aiming to construct complex molecules with precision and efficiency.