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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)-

(S)-N2-Boc-1-phenylethylenediamine

N[C@@H](c1ccccc1)CNC(=O)OC(C)(C)C Request for Quotation
Chemical Name: (S)-N2-Boc-1-phenylethylenediamine
CAS Number: 943322-87-0
Product Number: AG0032HG(AGN-PC-0WAFQN)
Synonyms:
MDL No:
Molecular Formula: C13H20N2O2
Molecular Weight: 236.3101

Identification/Properties

Properties
Storage:
Light sensitive;Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.315g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
236.152g/mol
Monoisotopic Mass:
236.152g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
242
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


(S)-tert-Butyl (2-amino-2-phenylethyl)carbamate is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique structure containing both an amino group and a carbamate moiety allows for a range of applications in the preparation of complex organic molecules.One of the key applications of (S)-tert-Butyl (2-amino-2-phenylethyl)carbamate is in asymmetric synthesis, where its chiral nature enables the creation of enantiomerically pure compounds. By utilizing this compound as a starting material, chemists can introduce chirality into target molecules with high selectivity, crucial for the pharmaceutical and agrochemical industries where enantiomeric purity is often required for optimal biological activity.Additionally, (S)-tert-Butyl (2-amino-2-phenylethyl)carbamate is utilized in the synthesis of peptide-based drugs and materials. Its amino and carbamate functionalities can be selectively modified and incorporated into peptide sequences, offering a valuable tool for the construction of peptide libraries or the preparation of peptide conjugates with specific properties.Furthermore, this compound serves as a protecting group in organic synthesis due to the stability of its carbamate moiety under a variety of reaction conditions. By strategically introducing and removing the (S)-tert-Butyl (2-amino-2-phenylethyl)carbamate group, chemists can control the reactivity and selectivity of functional groups in complex molecule synthesis.In summary, (S)-tert-Butyl (2-amino-2-phenylethyl)carbamate plays a crucial role in chemical synthesis by enabling the creation of chiral molecules, facilitating the preparation of peptide-based compounds, and providing protection for reactive functional groups. Its versatility and compatibility with a range of synthetic strategies make it a valuable tool for organic chemists working in diverse fields of research and development.