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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)-

Benzoic acid, 3-amino-, 1,1-dimethylethyl ester

Nc1cccc(c1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: Benzoic acid, 3-amino-, 1,1-dimethylethyl ester
CAS Number: 92146-82-2
Product Number: AG00GRVV(AGN-PC-0KK8I5)
Synonyms:
MDL No: MFCD00729048
Molecular Formula: C11H15NO2
Molecular Weight: 193.2423

Identification/Properties

Properties
MP:
81 °C
BP:
309.2 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
193.246g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
193.11g/mol
Monoisotopic Mass:
193.11g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
208
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


The tert-Butyl 3-aminobenzoate is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic molecules. It serves as a crucial intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of the tert-butyl group provides steric hindrance, which can influence the reactivity and selectivity of chemical reactions. This compound is particularly valuable in the synthesis of complex organic compounds due to its structural characteristics and reactivity profile. By utilizing tert-Butyl 3-aminobenzoate in chemical reactions, chemists can efficiently access diverse molecular structures with specific functional properties.