15089-51-7

Basic information

• Product Name: 4,5-Dimethylanthanilic acid
• Synonyms: 2-Amino-4,5-dimethylbenzoic acid;4,5-Dimethylanthanilic acid;4,5-Dimethyl-2-aminobenzoic acid;4,5-Dimethylanthranilic acid;NSC 104996;2-Carboxy-4,5-dimethylaniline
• CAS NO: 15089-51-7
• Molecular Formula: C₉H₁₁NO₂
• Molecular Weight: 165.19
• EINECS: 247-201-1
• Mol File: 15089-51-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 213-214 °C (decomp)
• Boiling Point: 341.656 °C at 760 mmHg
• Flash Point: 160.428 °C
• Appearance: /
• Density: 1.208 g/cm³
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 2.44±0.10(Predicted)
• CAS DataBase Reference: 4,5-Dimethylanthanilic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-Dimethylanthanilic acid(15089-51-7)
• EPA Substance Registry System: 4,5-Dimethylanthanilic acid(15089-51-7)

Safety Data

• Hazardous Substances Data: 15089-51-7(Hazardous Substances Data)

Usage

General Description

4,5-Dimethylanthanilic acid, also known as 4,5-dimethylaniline-2-carboxylic acid, is a chemical compound with the molecular formula C10H13NO2. It is derived from anthranilic acid, an aromatic amine commonly used in the production of dyes, pigments, and pharmaceuticals. 4,5-Dimethylanthanilic acid is a white crystalline solid that is sparingly soluble in water. It is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, including antihistamines, analgesics, and antimalarial drugs. 4,5-Dimethylanthanilic acid has also been studied for its potential biological activities, including anti-inflammatory and antioxidant properties, making it a molecule of interest in medicinal chemistry and drug development.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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.

Antihypertensive 2-amino-4(3H)-quinazolinones.

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