1. Home
  2. 4-[2-(Boc-amino)ethyl]aniline

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

4-[2-(Boc-amino)ethyl]aniline

O=C(OC(C)(C)C)NCCc1ccc(cc1)N Request for Quotation
Chemical Name: 4-[2-(Boc-amino)ethyl]aniline
CAS Number: 94838-59-2
Product Number: AG003KKY(AGN-PC-0WA9UF)
Synonyms:
MDL No:
Molecular Formula: C13H20N2O2
Molecular Weight: 236.3101

Identification/Properties

Properties
MP:
71 - 73°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.315g/mol
XLogP3:
2.2
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:
240
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The tert-Butyl 4-aminophenethylcarbamate is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound is commonly employed as a protecting group for amines in organic chemistry reactions. By selectively blocking the amine functional group with the tert-butyl 4-aminophenethylcarbamate, it prevents unwanted reactions or side products from occurring at that site during the synthesis process. This protective role allows chemists to manipulate other parts of the molecule without affecting the amine group, providing greater control and efficiency in the overall synthesis. Additionally, tert-Butyl 4-aminophenethylcarbamate can be selectively removed under specific conditions, enabling the desired target molecule to be obtained with the amine group restored. Its application in chemical synthesis demonstrates its crucial role in facilitating complex reactions and achieving high purity products.