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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, 3,5-bis(acetylamino)-

CC(=O)Nc1cc(NC(=O)C)cc(c1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 3,5-bis(acetylamino)-
CAS Number: 7743-39-7
Product Number: AG005LLV(AGN-PC-0JKX2R)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O4
Molecular Weight: 236.2240

Identification/Properties

Properties
MP:
>300°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.227g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
236.08g/mol
Monoisotopic Mass:
236.08g/mol
Topological Polar Surface Area:
95.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
305
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Diacetamidobenzoic acid, also known as DABA, is a versatile compound widely used in chemical synthesis. With its two acetamide functional groups, DABA serves as a crucial building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 3,5-Diacetamidobenzoic acid acts as a key intermediate for the synthesis of peptides and proteins. Its ability to introduce specific chemical functionalities allows for precise modification of amino acids during peptide synthesis. Furthermore, DABA can be utilized in the preparation of dendrimers, which are highly branched macromolecules with applications in drug delivery and materials science.Additionally, 3,5-Diacetamidobenzoic acid plays a significant role in the development of new materials with tailored properties. By incorporating DABA into polymer backbones, researchers can enhance the materials' thermal stability, solubility, and biocompatibility. This makes DABA a valuable tool for designing polymers for various industrial and biomedical applications.Overall, the application of 3,5-Diacetamidobenzoic acid in chemical synthesis enables the creation of complex molecules with specific functions and properties, making it a valuable tool for researchers and chemists in diverse fields.