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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)-

Benzeneacetamide,4-[(2S)-2-hydroxy-3-[(1-methylethyl)amino]propoxy]-

O[C@@H](CNC(C)C)CCc1ccc(cc1)CC(=O)N Request for Quotation
Chemical Name: Benzeneacetamide,4-[(2S)-2-hydroxy-3-[(1-methylethyl)amino]propoxy]-
CAS Number: 93379-54-5
Product Number: AG003CMV(AGN-PC-0W2XBN)
Synonyms:
MDL No:
Molecular Formula: C15H24N2O2
Molecular Weight: 264.3633

Identification/Properties

Properties
MP:
150 - 153°C
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
266.341g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
266.163g/mol
Monoisotopic Mass:
266.163g/mol
Topological Polar Surface Area:
84.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
263
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


(-)-Atenolol is a versatile chiral building block commonly used in chemical synthesis. Its unique stereochemistry makes it a valuable tool in asymmetric synthesis, where the creation of molecules with specific three-dimensional structures is crucial. In particular, (-)-Atenolol is often employed in the synthesis of pharmaceutical compounds and agrochemicals, where chirality plays a significant role in determining the biological activity and efficacy of the final product. By incorporating (-)-Atenolol into the synthetic pathway, chemists can access enantiopure molecules with enhanced selectivity and potency, making it a valuable asset in drug discovery and development.