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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-amino-4-(1,1-dimethylethyl)-, (S)-

OC[C@H](c1ccc(cc1)C(C)(C)C)N Request for Quotation
Chemical Name: Benzeneethanol, b-amino-4-(1,1-dimethylethyl)-, (S)-
CAS Number: 191109-50-9
Product Number: AG002F1Z(AGN-PC-0QK9EC)
Synonyms:
MDL No:
Molecular Formula: C12H19NO
Molecular Weight: 193.2854

Identification/Properties

Properties
MP:
115-119 °C
Storage:
Room Temperature;Light sensitive;Keep in dry area;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-(+)-2-Amino-2-(4-tert-butylphenyl)ethanol, also known as $name$, is a chiral compound widely utilized in chemical synthesis processes. Its unique stereochemistry and functional groups make it an essential building block in the development of various pharmaceuticals, advanced materials, and specialty chemicals.In organic synthesis, (S)-(+)-2-Amino-2-(4-tert-butylphenyl)ethanol serves as a valuable chiral auxiliary agent, enabling the selective creation of asymmetric structures. By harnessing its chirality, chemists can control the stereochemistry of reactions, leading to the formation of enantiomerically pure products with high optical purity. This compound is particularly valuable in the synthesis of complex molecules like pharmaceutical intermediates and agrochemicals, where precise stereochemical control is crucial for biological activity.Moreover, (S)-(+)-2-Amino-2-(4-tert-butylphenyl)ethanol can also act as a ligand in transition metal catalysis, facilitating various asymmetric transformations such as asymmetric hydrogenation, asymmetric allylation, and asymmetric Michael additions. Its coordination chemistry with transition metals enhances catalytic activity and selectivity, enabling the efficient synthesis of diverse organic compounds with high enantiomeric excess.In summary, (S)-(+)-2-Amino-2-(4-tert-butylphenyl)ethanol plays a pivotal role in chemical synthesis by enabling the construction of complex chiral molecules and facilitating selective asymmetric transformations. Its versatile applications make it a valuable tool for synthetic chemists seeking to access enantiomerically pure compounds for a wide range of industrial and research purposes.