15089-51-7

Usage

Uses

Used in Pharmaceutical Industry:
4,5-Dimethylanthanilic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its role in creating antihistamines, analgesics, and antimalarial drugs. Its structural properties allow for the development of compounds that target specific biological pathways, contributing to the treatment of a range of medical conditions.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 4,5-Dimethylanthanilic acid is utilized as an intermediate for the production of diverse organic compounds. Its unique structure facilitates the creation of new molecules with potential applications in various industries, including materials science and specialty chemicals.
Used in Medicinal Chemistry and Drug Development:
4,5-Dimethylanthanilic acid is studied for its potential biological activities, such as anti-inflammatory and antioxidant properties. These attributes make it a molecule of interest in medicinal chemistry, where it can be further explored and optimized for therapeutic applications, potentially leading to the development of new drugs with improved efficacy and safety profiles.

Upstream product

• 4315-14-4 4,5-Dimethyl-2-nitrobenzoesaeure 
• 15089-74-4 2-chloro-4,5-dimethylbenzoic acid 
• 676363-72-7 2-carbamoyl-4,5-dimethylbenzoic acid 
• 615-60-1 4-chloro-1,2-dimethylbenzene 
• 63920-72-9 6,7-dimethyl-1H-benzo[d][1,3]oxazine-2,4-dione 
• 28568-03-8 4,5-dimethyl-2-aminobenzonitrile 
• 6972-71-0 4,5-dimethyl-2-nitrobenzenamine 
• 15089-77-7 2,3-dimethyl-6-nitrobenzonitrile 
• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 20197-77-7 4,5-dimethyl-Δ⁴-tetrahydrophthalimide 
• 20197-78-8 5,6-dimethylisoindoline-1,3-dione 
• 2198-54-1 N-(3,4-dimethylphenyl)acetamide 
• 15089-73-3 1-(2-chloro-4,5-dimethyl-phenyl)-ethanone 

Downstream Products

• 56934-65-7 2-(Ethoxyoxalyl-amino)-4,5-dimethyl-benzoic acid 
• 19258-73-2 methyl 2-amino-4,5-dimethylbenzoate 
• 1094026-85-3 2-iodo-4,5-dimethylbenzaldehyde 
• 851384-78-6 (2-iodo-4,5-dimethylphenyl)methanol 

Relevant academic research and scientific papers

Rotational Control of a Dirhodium-Centered Supramolecular Four-Gear System by Ligand Exchange

Self-assembled molecular machines have great potential to enable noncovalent regulation of a coupled motion of the building blocks. Herein we report the synthesis and the rotational control of a lantern-type dirhodium complex with circularly arranged four

Molecular Crystals with Moving Parts: Synthesis, Characterization, and Crystal Packing of Molecular Gyroscopes with Methyl-Substituted Triptycyl Frames

We report a highly convergent synthesis for the preparation of molecular gyroscopes consisting of para-phenylene rotors linked by triple bonds to methyl-substituted triptycenes acting as pivots and encapsulating frames. The desired 1,4-bis[2-(2,3,6,7,12,1

FUSED-RING PYRIMIDIN-4(3H)-ONE DERIVATIVES, PROCESSES FOR THE PREPARATION AND USES THEREOF

AbstractNovel compounds of the following formula (I) and pharmacologically acceptable salt and esters thereof can modulate LXR function and as a result show excellent anti-arteriosclerotic and anti-inflammatory activity:wherein:A represents aryl or heteroaryl;R1, R2 and R3 are the same or different and each represents hydrogen, hydroxyl, nitro, cyano, amino, halogen, carboxy, carbamoyl, mercapto, alkyl, haloalkyl, alkylcarbonyloxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, N-(alkylcarbonyl)-N-(alkyl)amino, alkoxycarbonylamino, N-(alkoxycarbonyl)-N-(alkyl)amino, alkylsulfonylamino, N-(alkylsulfonyl)-N-(alkyl)amino, haloalkylsulfonylamino, N-(haloalkylsulfonyl)-N-(alkyl)amino, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl or dialkylaminocarbonyl group, or R1 and R2 together are alkylenedioxy;R4 and R5 are the same or different and each represents hydrogen, hydroxyl, amino, halogen, mercapto, alkyl, haloalkyl, alkoxy, alkoxycarbonyl or alkylthio;X represents hydrogen, hydroxyl, halogen, alkoxy or haloalkoxy; andY represents an optionally substituted alkyl, cycloalkyl, heterocyclyl, aryl, cycloalkylalkyl, heterocyclylalkyl or aralkyl group.

N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors

Described are compounds of formula (I), wherein W is O or S; X is NR8; Y is CR9R10-(CH2)n wherein R9 and R10 are independently of each other hydrogen or lower alkyl, and n is an integer of