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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)-

tert-butyl N-[2-amino-2-(4-cyanophenyl)ethyl]carbamate;hydrochloride

NC(c1ccc(cc1)C#N)CNC(=O)OC(C)(C)C.Cl Request for Quotation
Chemical Name: tert-butyl N-[2-amino-2-(4-cyanophenyl)ethyl]carbamate;hydrochloride
CAS Number: 939760-53-9
Product Number: AG003CR2(AGN-PC-0JCVVD)
Synonyms:
MDL No:
Molecular Formula: C14H20ClN3O2
Molecular Weight: 297.7805

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
297.783g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
297.124g/mol
Monoisotopic Mass:
297.124g/mol
Topological Polar Surface Area:
88.1A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
345
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (2-amino-2-(4-cyanophenyl)ethyl)carbamate is a versatile compound that finds application in various chemical synthesis processes. Due to its unique structure and reactivity, this compound is commonly used as a protecting group in organic synthesis. By selectively masking specific functional groups in a molecule, the tert-Butyl (2-amino-2-(4-cyanophenyl)ethyl)carbamate can help to control the reactivity of certain sites during a chemical reaction. This selective protection allows chemists to perform complex multi-step reactions with greater precision and efficiency. Additionally, the tert-Butyl (2-amino-2-(4-cyanophenyl)ethyl)carbamate can serve as a precursor for the synthesis of other important compounds, making it a valuable building block in the development of new materials and pharmaceuticals.