(S)-3-Amino-2-(benzylamino)propan-1-ol|1260587-77-6,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

(S)-3-Amino-2-(benzylamino)propan-1-ol

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Chemical Name:	(S)-3-Amino-2-(benzylamino)propan-1-ol
CAS Number:	1260587-77-6
Product Number:	AG000QUU(AGN-PC-0WAGR9)
Synonyms:
MDL No:
Molecular Formula:	C10H16N2O
Molecular Weight:	180.2468

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Chemical Structure

(S)-3-Amino-2-(benzylamino)propan-1-ol is a versatile compound widely utilized in chemical synthesis for a variety of applications. This chiral aminoalcohol compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its asymmetric nature allows for precise control over the stereochemistry of target molecules, making it a critical component in the synthesis of enantiomerically pure compounds. In the realm of drug discovery and development, (S)-3-Amino-2-(benzylamino)propan-1-ol plays a vital role in the creation of biologically active compounds with enhanced potency and selectivity. Its unique structure lends itself well to the creation of complex molecules through strategic manipulation of its functional groups. Additionally, this compound can be employed as a catalyst or ligand in asymmetric synthesis reactions, facilitating the formation of highly enantioenriched products. Its broad synthetic utility and ability to impart chirality make (S)-3-Amino-2-(benzylamino)propan-1-ol an indispensable tool for modern organic chemistry.