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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)-

Carbamic acid, (2-aminophenyl)-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)Nc1ccccc1N Request for Quotation
Chemical Name: Carbamic acid, (2-aminophenyl)-, 1,1-dimethylethyl ester
CAS Number: 146651-75-4
Product Number: AG007J2Q(AGN-PC-0JUSLJ)
Synonyms:
MDL No:
Molecular Formula: C11H16N2O2
Molecular Weight: 208.2569

Identification/Properties

Computed Properties
Molecular Weight:
208.261g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
208.121g/mol
Monoisotopic Mass:
208.121g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
223
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl (2-aminophenyl)carbamate, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key building block for organic molecules. Its strategic incorporation in synthetic routes allows for the efficient formation of diverse chemical structures with tailored properties, making it a valuable tool in the hands of synthetic chemists. This compound serves as a crucial intermediate in the synthesis of various biologically active compounds, pharmaceuticals, and advanced materials. Due to its unique structural features, $name$ enables chemists to introduce specific functionalities and stereochemical elements into their target molecules, facilitating the design and development of novel compounds with desired properties. In the realm of chemical synthesis, the application of tert-Butyl (2-aminophenyl)carbamate plays a pivotal role in advancing the frontier of organic chemistry and driving innovation in the field.