29455-11-6

Usage

Uses

Used in Chemical Synthesis Industry:
4-Methoxy-3,5-dinitrotoluene is used as a chemical intermediate for the production of dyes, pigments, and pharmaceuticals, contributing to the coloration and medicinal properties of various products.
Used in Explosives and Propellants Industry:
Leveraging its explosive properties, 4-Methoxy-3,5-dinitrotoluene is utilized in the manufacturing of explosives and propellants, enhancing the performance and efficiency of these materials in various applications.

InChI:InChI=1/C8H8N2O5/c1-5-3-6(9(11)12)8(15-2)7(4-5)10(13)14/h3-4H,1-2H3

Upstream product

• 186581-53-3 diazomethane 
• 609-93-8 2,6-dinitro-p-cresol 
• 104-93-8 p-methylanizole 
• 119-10-8 4-methoxy-3-nitrotoluene 
• 108-24-7 acetic anhydride 
• 5264-65-3 3,5-Dinitro-4-chlorotoluene 
• 124-41-4 sodium methylate 
• 74-88-4 methyl iodide 
• 725232-33-7 4-methyl-6-tert-butyl-2-nitroanisole 
• 7697-37-2 nitric acid 
• 119-33-5 4-methyl-2-nitrophenol 
• 106-49-0 p-toluidine 
• 67-56-1 methanol 

Downstream Products

• 37780-40-8 2-methoxy-5-methyl-benzene-1,3-diamine 
• 499979-63-4 N,N'-bis-(4-methyl-2,6-dinitro-phenyl)-propanediyldiamine 
• 83604-27-7 2-methoxy-3-nitro-5-methylaniline 
• 6393-42-6 4-methyl-2,6-dinitroaniline 
• 861362-41-6 N-(4-methyl-2,6-dinitro-phenyl)-hydroxylamine 
• 83757-30-6 2,6-dinitro-4-methyl-N-(β-hydroxypropyl)-aniline 
• 83757-29-3 2,6-dinitro-4-methyl-N-(β,γ-dihydroxypropyl)-aniline 
• 83604-29-9 1,3-bis(2-methoxy-3-nitro-5-methylphenyl)tetrahydro-2(1H)-pyrimidinone 
• 83604-28-8 1,3-bis(2-methoxy-3-nitro-5-methylphenyl)urea 
• 91084-79-6 1,3-bis(2-methoxy-3-amino-5-methylphenyl)tetrahydro-2(1H)-pyrimidinone 
• 84011-90-5 33,35,37-trioxo-34,38-dimethoxy-4,26-dimethyl-36-<3-(methoxymethyl)phenyl>-1,7,11,19,23,29-hexaazaheptacyclo<27.3.1.1^2,6.1^7,11.1^13,17.1^19,23.1^24,28>octaconta-34(2),3,5,36(13),14,16,38(24),25,27-nonaene 
• 83604-32-4 1,3-bis<2-methoxy-3-(1-tetrahydro-(3H)-pyrimidinonyl)-5-methylphenyl>tetrahydro-2(1H)-pyrimidinone 
• 84379-43-1 2,6-bis(hexahydro-2-oxopyrimidinyl)-4-methylbenzene 
• 92185-85-8 1-(3-Chloro-propyl)-3-{3-[3-(3-chloro-propyl)-ureido]-2-methoxy-5-methyl-phenyl}-urea 

Relevant academic research and scientific papers

ipso NITRATION. XXIX. NITRATION OF SUBSTITUTED 4-METHYLANISOLES AND PHENOLS

Nitration of 2-chloro-4-methylanisole (1a) in acetic anhydride gives (Z)-4-chloro-3-methoxy-6-methyl-6-nitrocyclohexa-2,4-dienyl acetate (2a), 2-chloro-4-methyl-4-nitrocyclohexa-2,5-dienone (3a), and 2-chloro-4-methyl-6-nitroanisole (4a).Similarly 2-bromo-4-methylanisole (1b) gives (Z)-4-bromo-3-methoxy-6-methyl-6-nitrocyclohexa-2,4-dienyl acetate (2b), 2-bromo-4-methyl-4-nitrocyclohexa-2,5-dienone (3b), and 2-bromo-4-methyl-6-nitroanisole (4b), whereas 4-methyl-2-nitro-anisole (1c) gives (Z)-3-methoxy-6-methyl-4,6-dinitrocyclohexa-2,4-dienyl acetate (2c), (Z)-3-methoxy-6-methyl-2,6-dinitrocyclohexa-2,4-dienyl acetate (7), and 4-methyl-2,6-dinitroanisole (4c).Nitration of 3-chloro-4-methylanisole (9a) gives 3-chloro-4-methyl-4-nitrocyclohexa-2,5-dienone (10a), 3-chloro-4-methyl-2-nitro anisole (11a), and 5-chloro-4-methyl-2-nitroanisole (12a), and 4-methyl-3-nitroanisole (9c) gives (Z)-3-methoxy-6-methyl-5,6-dinitrocyclohexa-2,4-dienyl acetate (13), 4-methyl-2,3-dinitroanisole (11c), and 4-methyl-2,5-dinitroanisole (12c).Nitration of 2-chloro-4-methylphenol (14) in chloroform gives 3a and 2-chloro-4-methyl-6-nitrophenol (5a), and 3-chloro-4-methylphenol (15) gives dienone 10a, 3-chloro-4-methyl-2-nitrophenol (16), and 5-chloro-4-methyl-2-nitrophenol (17).