69051-75-8

Basic information

• Product Name: 4,6-dimethyl-2-nitroanisole
• Synonyms: 4,6-dimethyl-2-nitroanisole
• CAS NO: 69051-75-8
• Molecular Weight: 181.191
• Mol File: 69051-75-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4,6-dimethyl-2-nitroanisole(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-dimethyl-2-nitroanisole(69051-75-8)
• EPA Substance Registry System: 4,6-dimethyl-2-nitroanisole(69051-75-8)

Safety Data

• Hazardous Substances Data: 69051-75-8(Hazardous Substances Data)

Upstream product

• 14452-34-7 2,4-dimethyl-6-nitrophenol 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 
• 509-14-8 tetranitromethane 
• 6738-23-4 2,4-dimethylanisole 
• 105-67-9 2,4-Xylenol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 35490-72-3 2-methoxy-3,5-dimethylaniline 
• 2785-85-5 2-methoxy-3,5-dimethylphenol 
• 2785-75-3 3,5-dimethylcatechol 
• 67618-05-7 1-(2-Methoxy-3,5-dimethylphenyl)-thioharnstoff 

Relevant articles and documents

COUMARIN DERIVATIVES AND METHODS OF USE IN TREATING CYSTIC FIBROSIS, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, AND MISFOLDED PROTEIN DISORDERS

Novel CFTR corrector compounds that are effective in rescuing halide efflux, delF508-CFTR protein processing, and apical functional chloride ion transport in a cell are provided. Also provided are methods for treating protein folding disorders (e.g., cyst

Photochemical nitration by tetranitromethane. Part XXXVII. Adduct formation and the regiochemistry of attack of trinitromethanide ion on radical cations in the photochemical reactions of 2-methyl-, 2,3-dimethyl- and 2,4-Dimethylanisoles

The photolysis of the charge transfer (CT) complex of tetranitromethane and 2-methylanisole 2 in dichloromethane at 20 °C gives the epimeric 1-methoxy-6-methyl-6-nitro-3-trinitromethylcyclohexa-1,4-dienes 8 and 9 in addition to 2-methyl-4-trinitromethylanisole (3) and 2-methyl-4-nitroanisole (4). In acetonitrile the yields of compound 4 and adducts 8 and 9 are significantly higher. Similar reaction of 2,3-dimethylanisole (6) in dichloromethane gave nitro-trinitromethyl adducts 10 and 11, hydroxy-trinitromethyl adducts 12 and 13, 2,3-dimethyl-5-trinitromethylanisole (14), 4-methoxy-2,3-dimethylbenzonitrile N-oxide (15), 2,3-dimethyl-4-trinitromethylanisole (16), 2,3-dimethyl-4-nitroanisole (17), 2,3-dimethyl-4,6-dinitrophenol (18), 3-methoxy-4,5-dimethyl-benzoic acid (19) and the hydroxy dinitro compound (20). The photolysis of the CT complex of 2,4-dimethylanisole (7) with tetranitromethane in dichloromethane gave the epimeric 1-methoxy-4,6-dimethyl-6-nitro-3-trinitromethylcyclohexa-1,4-dienes 21 and 22, together with 4,6-dimethyl-3-trinitromethylanisole (23), 4,6-dimethyl-2-nitrophenol (24), 4,6-dimethyl-2-trinitromethylanisole (25), 4,6-dimethyl-3-nitroanisole (26), 4,6-dimethyl-2-nitroanisole (27) and 4,6-dimethyl-4-nitrocyclohexa-2,5-dienone (28). The modes of formation of the above products are discussed, including the effects of the reaction solvent on those processes. The X-ray crystal structure of 1-methoxy-2-methyl-c-6-nitro-r-3-trinitromethylcyclohexa-1,4-diene (9) is reported. Acta Chemica Scandinavica 1997.

Tobacco smoke chemistry. 2. Alkyl and alkenyl substituted guaiacols found in cigarette smoke condensate.

A series of alkyl and alkenyl substituted guaiacols, which comprise a group of biologically and organoleptically active compounds, have been synthesized. Mass spectra and GC retention times for these have been recorded and compared with those obtained for constituents of a weakly acidic fraction of smoke condensate derived from American blend type cigarettes. On the basis of these results, 25 guaiacols have been identified, 18 of which have not been detected in tobacco smoke condensate previously.