41864-45-3

Basic information

• Product Name: 4,5-DIMETHOXY-2-METHYLANILINE
• Synonyms: 4,5-DIMETHOXY-2-METHYL-PHENYLAMINE;4,5-DIMETHOXY-2-METHYLANILINE;4,5-dimethoxy-2-methylbenzenamine;4,5-dimethoxy-2-methylaniline hydrochloride;2-Methyl-4,5-dimethoxyaniline;NSC 105305;4,5-Dimethoxy-2-methylaniline 2-Methyl-4,5-dimethoxyaniline
• CAS NO: 41864-45-3
• Molecular Formula: C₉H₁₃NO₂
• Molecular Weight: 167.21
• Mol File: 41864-45-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 108-110°C
• Boiling Point: 283.7 °C at 760 mmHg
• Flash Point: 136.2 °C
• Appearance: /
• Density: 1.072 g/cm³
• Vapor Pressure: 0.00311mmHg at 25°C
• Refractive Index: 1.536
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.63±0.10(Predicted)
• CAS DataBase Reference: 4,5-DIMETHOXY-2-METHYLANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-DIMETHOXY-2-METHYLANILINE(41864-45-3)
• EPA Substance Registry System: 4,5-DIMETHOXY-2-METHYLANILINE(41864-45-3)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39-22
• HazardClass: IRRITANT, IRRITANT-HARMFUL
• Hazardous Substances Data: 41864-45-3(Hazardous Substances Data)

Usage

General Description

4,5-Dimethoxy-2-methylaniline is a chemical compound primarily defined by its three key structural components: two methoxy groups (OCH3) attached at the 4th and 5th positions, a methyl group (CH3) at the 2nd position, and an aniline functional group (NH2) at the end. These constituents grant the compound certain characteristics that make it useful for various purposes. In terms of its physical properties, it appears as a light yellow, crystalline solid under normal conditions. It has a specific molecular formula of C10H15NO2 and holds a molecular weight of approximately 179.23 g/mol. Notably, this compound can be potentially hazardous, based on its associated hazard statements and safety precautions. Its uses, while not widely stated, often pertain to the realm of organic synthesis and chemical research due to its reactive nature.

InChI:InChI=1/C9H13NO2/c1-6-4-8(11-2)9(12-3)5-7(6)10/h4-5H,10H2,1-3H3

Upstream product

• 7509-11-7 1,2-dimethoxy-4-methyl-5-nitrobenzene 

Downstream Products

• 749819-92-9 4-amino-5-methyl-pyrocatechol 
• 860369-12-6 4-Amino-2-methoxy-5-methyl-phenol 
• 856181-38-9 5-Amino-2-methoxy-4-methyl-phenol 
• 408509-80-8 4,5-dimethoxy-N,2-dimethylaniline 
• 58814-69-0 4,5-dimethoxy-2-methyl-benzonitrile 
• 614-13-1 2-methoxy-5-methyl-1,4-benzoquinone 
• 101599-65-9 N-(4,5-Dimethoxy-2-methyl-phenyl)-imino-bernsteinsaeure-diethylester 
• 28046-47-1 N,N'-Bis-4,5-dimethoxy-o-tolyloxamid 
• 30072-80-1 N-(2-Diethylamino-ethyl)-N-(4,5-dimethoxy-2-methyl-phenyl)-N',N'-diethyl-ethane-1,2-diamine 
• 20736-28-1 4,5-dimethoxy-2-methylbenzoic acid 
• 577-68-4 m-hemipinic acid 
• 500766-29-0 N₄-(5-tert-butylisoxazol-3-yl)-N₂-(4,5-dimethoxy-2-methyl-phenyl)-pyrimidine-2,4-diamine 
• 500766-44-9 N₂-(2-methyl-4,5-dimethoxyphenyl)-N₄(5-phenylisoxazol-3-yl)-2,4-pyrimidinediamine 
• 438248-93-2 4-(4,5-Dimethoxy-2-methylanilino)-2-(3-pyridinyl)-6-(trifluoromethyl)pyrimidine 

Relevant articles and documents

:[Reductive degradation of glycine and o-quinone addition products]

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Multisubstituted 1-hydroxy-9-acridones with anticancer activity

The present invention provides a compound having the structure: STR1 The present invention also provides a method for synthesizing a compound having the above-identified structure as well as the intermediate compounds produced according to that method. The present invention further provides a pharmaceutical composition comprising the above compounds. Lastly, the present invention provides a method of inhibiting growth of tumor cells.