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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, (4-aminophenyl)-, 1,1-dimethylethyl ester

O=C(Nc1ccc(cc1)N)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, (4-aminophenyl)-, 1,1-dimethylethyl ester
CAS Number: 71026-66-9
Product Number: AG003KAG(AGN-PC-0JUYNZ)
Synonyms:
MDL No:
Molecular Formula: C11H16N2O2
Molecular Weight: 208.2569

Identification/Properties

Properties
MP:
113°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
208.261g/mol
XLogP3:
1.5
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:
215
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-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Carbamic acid, N-(4-aminophenyl)-, 1,1-dimethylethyl ester is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique chemical properties. As a key intermediate in organic synthesis, it serves as a building block for the development of complex molecules with specific biological activities. Its strategic incorporation into synthetic pathways enables the efficient production of a diverse range of compounds with tailored functionalities. Researchers and chemists leverage the reactivity of Carbamic acid, N-(4-aminophenyl)-, 1,1-dimethylethyl ester to facilitate the synthesis of novel compounds that exhibit promising properties for various applications in the fields of medicine, agriculture, and materials science.