4-Acetyl-2-methylbenzoic acid

Product Details

CAS No:55860-35-0

MF:C10H10O3

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

Package:25kgs/drum

Supply Capacity:Tons

Synonyms:4-acetyl-2-methylbenzoic acid;Benzoic acid, 4-acetyl-2-methyl-;4-acetyl-2-methylbenzoic acid ISO 9001：2015 REACH;Fluralaner intermediate;2-methyl-4-acetyl-enzoic acid;Fluralaner Impurity 27;Flurellana Impurity 1;4 cetyl-2-methylbenzoic acid; 4-acetyl-2-methylbenzoic acid; 55860-35-0; RefChem:517316; 856-079-4; MFCD20639525; 4-Acetyl-2-methylbenzoicacid; 4-acetyl-2-methyl-benzoic acid; SCHEMBL2012610; AC-37199; CS-0112809; F53493; orb3144253; WLZ3526; TYD-03594; SY342262; DB-087369; F612746; A1-08799

Product application:4-Acetyl-2-methylbenzoic acid,55860-35-0,4-Acetyl-o-toluic acid,2-Methyl-4-acetylbenzoic acid,p-Acetyl-o-toluic acid,Pharmaceutical grade 4-Acetyl-2-methylbenzoic acid,Isoxazoline veterinary drug intermediate,Afoxolaner intermediate,Sarolaner intermediate,Ectoparasiticide synthon,Aromatic keto acid building block,Fine organic chemical intermediate,Anti-inflammatory API intermediate,Specialty photosensitive monomer,High purity 4-Acetyl-2-methylbenzoic acid 99.5%,CAS 55860-35-0 supplier,4-Acetyl-2-methylbenzoic acid manufacturer China,Suzhou Health Chemicals specialty chemicals,4-Acetyl-2-methylbenzoic acid wholesale bulk export

 

4-Acetyl-2-methylbenzoic acid serves as an indispensable, ultra-pure bifunctional aromatic keto acid building block, benchmark veterinary pharmaceutical active pharmaceutical ingredient (API) intermediate, and versatile fine organic synthon extensively utilized across modern companion animal ectoparasiticide manufacturing, novel anti-inflammatory and oncology drug discovery, and specialty functional polymer engineering sectors. In animal health sciences and veterinary pharmaceutical process research, universally designated as 4-acetyl-o-toluic acid, its molecular architecture incorporates both an aromatic carboxylic acid group and an electrophilic acetyl moiety across a substituted benzene core bearing an ortho-methyl substituent; this dual functional arrangement enables highly chemoselective derivatization, such as selective amide bond formation or condensation, where the steric profile of the adjacent methyl group restricts conformational rotation to enhance receptor-binding complementarity within invertebrate neural targets; this molecular configuration optimizes lipophilicity and resists metabolic clearance pathways in target pharmaceuticals, extending therapeutic half-life and efficacy. In human medicinal chemistry, it functions as a versatile synthon for the synthesis of targeted kinase inhibitors, non-steroidal anti-inflammatory analogues, and peptidomimetic core structures. In specialty materials science and photo-curing polymer chemistry, the aromatic keto-carbonyl group provides intrinsic ultraviolet-sensitive photoreactivity, facilitating the formulation of high-performance polyaramids, liquid-crystalline polyesters, and specialized photoresist additives with elevated thermal stability. Furthermore, in weather-resistant organic pigment modification, chiral ligand coordination frameworks, and high-performance industrial barrier resins, chemical systems engineered from 4-Acetyl-2-methylbenzoic acid deliver exceptional reaction selectivity, crystalline reproducibility, and broad multi-industry performance.