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1,4 Dimethoxybenzene

The cyclic carbonate is easily cleaved by refluxing in water for 30 min. It can be converted to the 1,2-dimethoxybenzene derivative (aq. NaOH, Me2S04, reflux, 3 h). ... [Pg.173]

Dendrimer 1 + is a classical example of a dendrimer containing a luminescent metal complex core. In this dendrimer the 2,2 -bipyridine (bpy) ligands of the [Ru(bpy)3] +-type core carry branches containing 1,2-dimethoxybenzene- and 2-naphthyl-type chromophoric units [15]. [Pg.163]

Kwok ESC, R Atkinson, J Arey (1995) Rate constants for the gas-phase reactions of the OH radical with dichlorobiphenyls, 1-chlorodibenzo-p-dioxin, 1,2-dimethoxybenzene, and diphenyl ether estimation of OH radical reaction rate constants for PCBs, PCDDs, and PCDFs. Environ Sci Technol 29 1591-1598. [Pg.43]

Urticants are relatively unstable and tend to decompose spontaneously unless stored at low temperatures. Below —4°F, they can be kept for extended periods. Solvents including 1, 2-dimethoxybenzene, ether, dioxane, nitromethane, and glycine act as stabilizers and may be added to help prevent decomposition of agents during storage. Agents can be stored in glass or enamel-lined containers. Urticants rapidly attack rubber and metals, especially iron. [Pg.209]

The photochemical deprotection of sulphonamides to free amines is synthetically useful193. This process is caused by electron transfer from an electron-donating sensitizer such as 1,2-dimethoxybenzene or 1,4-dimethoxybenzene and the presence of reductants like ammonia or hydrazine is also required194 (equation 139). [Pg.736]

All the 3-diazoindazoles 2, irradiated in an aromatic solvent (benzene, p-chlorotoluene, benzonitrile, 1,2-dimethoxybenzene), gave by ring substitution the corresponding 3-arylindazoles in variable yields (66LA17). 3-Diazoindazole 2b, irradiated in pyridine and in thiophene, gave the 6-chloro-3-(2-pyridyl)-indazole and the 6-chloro-3-(2- or 3-thiophenyl)-indazole (66LA17). [Pg.102]

Detailed NMR and theoretical studies have identified and characterized a number of the complexes along the proposed reaction pathways for anisole, 1,2-dimethoxybenzene and Al,Al-dimethylaniline ° . For example, anisole deaggregates the BuLi hexamer to form a tetrameric BuLi-anisole complex 4. Adding TMEDA displaces the anisole from the tetramer and breaks it down further to give a BuLi-TMEDA dimer 5, which deprotonates anisole at >0°C yielding 6 (Scheme 4). [Pg.498]

Preparation of hexamethyl orthomuconate by the electrochemical methoxylation of 1,2-dimethoxybenzene [190],... [Pg.292]

Efficient synthesis of 6,7-dimethoxybenzopentathiepin 102 and 6-(2-aminoethyl)benzopentathiepin 103 (Figure 29), which are sectional structures of varacin, were proposed from 1,2-dimethoxybenzene and 1,2-benzene-dithiol, respectively <1995H(41)893>. [Pg.556]


See other pages where 1,4 Dimethoxybenzene is mentioned: [Pg.453]    [Pg.472]    [Pg.550]    [Pg.591]    [Pg.1081]    [Pg.320]    [Pg.156]    [Pg.243]    [Pg.268]    [Pg.565]    [Pg.214]    [Pg.478]    [Pg.221]    [Pg.189]    [Pg.722]    [Pg.741]    [Pg.819]    [Pg.1350]    [Pg.228]    [Pg.126]    [Pg.1237]    [Pg.54]    [Pg.200]    [Pg.202]    [Pg.193]    [Pg.589]    [Pg.302]    [Pg.320]    [Pg.74]    [Pg.346]    [Pg.628]    [Pg.655]    [Pg.424]    [Pg.439]    [Pg.211]    [Pg.512]    [Pg.513]    [Pg.513]    [Pg.576]    [Pg.614]   
See also in sourсe #XX -- [ Pg.400 ]

See also in sourсe #XX -- [ Pg.599 ]

See also in sourсe #XX -- [ Pg.49 ]

See also in sourсe #XX -- [ Pg.2 , Pg.13 ]




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1,2-Dimethoxybenzene, reactions with

1,4-dimethoxybenzene, 1,4-addition

1- iodo-2,3-dimethoxybenzene

1-Vinyl-3,4-dimethoxybenzene

1.2- Dimethoxybenzene, pyridination

1.3- Dimethoxybenzene bromination

1.3- Dimethoxybenzene, reaction with sulfur

1.4- Dichloro-2,5-dimethoxybenzene

1.4- Dimethoxybenzene benzoyl chloride

1.4- Dimethoxybenzene hydroquinone dimethyl ether

1.4- Dimethoxybenzene, nitration

1.4- dibromo-2,5-dimethoxybenzene

1.4- dimethoxybenzene (DMB

1.4- dimethoxybenzene absorption

2- Chloro-l ,4-dimethoxybenzene

2.4- dimethoxybenzene-, sodium

4- Bromo-1,2-dimethoxybenzene

4-Allyl-l,2-dimethoxybenzene

Benzenes Dimethoxybenzenes

Dimethoxybenzene ligand

Dimethoxybenzene units

Dimethoxybenzenes

Dimethoxybenzenes

M-dimethoxybenzene

O-Dimethoxybenzene

P-Dimethoxybenzene

Prenylation methods of 1,3-dimethoxybenzene

Veratrole (1,2-Dimethoxybenzene)

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