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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, a-(methylamino)-

CNC(c1ccccc1)C(=O)O Request for Quotation
Chemical Name: Benzeneacetic acid, a-(methylamino)-
CAS Number: 74641-60-4
Product Number: AG005VXG(AGN-PC-0U5RQ6)
Synonyms:
MDL No:
Molecular Formula: C9H11NO2
Molecular Weight: 165.1891

Identification/Properties

Properties
MP:
245-246℃
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
165.192g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
165.079g/mol
Monoisotopic Mass:
165.079g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
153
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Methylamino)-2-phenylacetic acid, also known as MAPA, plays a crucial role in chemical synthesis as a versatile building block. This compound serves as a valuable intermediate in the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. With its unique structure, MAPA offers a wide range of synthetic possibilities, allowing chemists to introduce specific functionalities and stereochemistry into target molecules.In organic synthesis, MAPA can be utilized as a chiral auxiliary for asymmetric transformations, enabling the creation of enantiomerically pure compounds. Its incorporation into the structure of complex molecules can facilitate the control of stereochemistry during key bond-forming reactions. Additionally, MAPA can serve as a precursor for the synthesis of diverse heterocyclic compounds, which are prevalent in pharmaceutical and agrochemical research.Furthermore, MAPA's ability to undergo various functional group modifications makes it a valuable tool for derivatization strategies in chemical synthesis. Chemists can efficiently transform the methylamino and phenyl groups of MAPA into different functional groups, thereby expanding the compound's synthetic applications. Overall, the strategic incorporation of 2-(Methylamino)-2-phenylacetic acid in chemical reactions offers synthetic chemists a powerful means to access structurally diverse and biologically active compounds.