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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)-

Benzeneacetic acid, 2-amino-

OC(=O)Cc1ccccc1N Request for Quotation
Chemical Name: Benzeneacetic acid, 2-amino-
CAS Number: 3342-78-7
Product Number: AG00BXBZ(AGN-PC-0JTAIA)
Synonyms:
MDL No:
Molecular Formula: C8H9NO2
Molecular Weight: 151.1626

Identification/Properties

Properties
MP:
123-127 °C(lit.)
BP:
344.4°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
151.165g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
151.063g/mol
Monoisotopic Mass:
151.063g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
147
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-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzeneacetic acid, 2-amino-, is a versatile compound widely used in chemical synthesis for its key role as a building block in the creation of various organic molecules. With its amino group and aromatic ring structure, this compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other complex organic compounds. By participating in a range of chemical reactions, including acylation, amidation, and condensation processes, Benzeneacetic acid, 2-amino-, facilitates the formation of diverse functional groups and molecular structures essential for the development of innovative materials and biologically active compounds. Its strategic placement within a molecule allows for the introduction of specific functionalities, enabling chemists to tailor the properties and functions of target compounds with precision. This compound's versatility and importance in chemical synthesis make it a valuable tool in the hands of synthetic chemists striving to create novel molecules with unique properties and applications.