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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)-

4-amino-2,5-dimethyl-benzoic acid

Cc1cc(C(=O)O)c(cc1N)C Request for Quotation
Chemical Name: 4-amino-2,5-dimethyl-benzoic acid
CAS Number: 21339-73-1
Product Number: AG007QS8(AGN-PC-0JNSJP)
Synonyms:
MDL No:
Molecular Formula: C9H11NO2
Molecular Weight: 165.1891

Identification/Properties

Computed Properties
Molecular Weight:
165.192g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
165.079g/mol
Monoisotopic Mass:
165.079g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
181
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Amino-2,5-dimethylbenzoic acid, also known as o-aminomethyl m-xylene acid, is a versatile compound widely used in chemical synthesis. With its unique chemical properties, this compound plays a crucial role in various reactions and processes in the field of organic chemistry.One of the key applications of 4-Amino-2,5-dimethylbenzoic acid is as a building block in the synthesis of pharmaceuticals and agrochemicals. Its structural characteristics allow it to be easily incorporated into complex molecular structures, making it an essential intermediate in the production of a wide range of bioactive compounds.Furthermore, this compound is utilized in the preparation of dyes and pigments due to its ability to contribute to the color and stability of the final products. By participating in specific chemical reactions, 4-Amino-2,5-dimethylbenzoic acid enables the formation of chromophores and functional groups essential for the coloration and performance of dyes and pigments.In addition, 4-Amino-2,5-dimethylbenzoic acid serves as a valuable reagent in the synthesis of specialty chemicals and materials. Its reactivity and compatibility with various functional groups make it an ideal starting material for the creation of advanced polymers, coatings, and other high-value products.Overall, the significance of 4-Amino-2,5-dimethylbenzoic acid in chemical synthesis lies in its role as a versatile and indispensable building block for the preparation of pharmaceuticals, agrochemicals, dyes, pigments, specialty chemicals, and materials. Its diverse applications contribute to the advancement of numerous industries and the development of innovative chemical products.