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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)-

Benzeneethanol, b-[(phenylmethyl)amino]-, (bR)-

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Chemical Name: Benzeneethanol, b-[(phenylmethyl)amino]-, (bR)-
CAS Number: 14231-57-3
Product Number: AG003C44(AGN-PC-0PS79D)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
BP:
87-90 °C(lit.)
Storage:
Room Temperature;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
227.307g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
227.131g/mol
Monoisotopic Mass:
227.131g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
195
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


(R)-(-)-N-Benzyl-2-phenylglycinol, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. This chiral auxiliary plays a crucial role in asymmetric synthesis, specifically in the preparation of enantiomerically pure compounds. By incorporating (R)-(-)-N-Benzyl-2-phenylglycinol into a synthetic pathway, chemists can control the stereochemistry of the final product, leading to desired chirality outcomes. Additionally, this compound is frequently employed in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules where chirality is a determining factor in biological activity or function. Its strategic use in asymmetric transformations makes it a valuable tool for achieving high levels of selectivity and efficiency in organic synthesis processes.