Bromo nitro-benzenes

Bromo methylbenzoic acid isobutyl ester fenpyroximate p Bromo nitro benzene chlorbromuron 4 Bromophenol silafluofen a Bromo a phenyl acetone diphacinone Bromo pinacolone diclobutrazol, triadimefon Bromo propane penconazole... 

Ethanone, 1- [3-(l,l-dimethylethyl)-4-methoxy-5-nitrophenyl Benzaldehyde, 2 (l,l-dimethylethyl)-4-methoxy-5-nitro Benzene, 1,4-BIS- (1, l-dimethylethyl)-2 methoxy-5-nitro Benzene, 1-(1, l-dimethylethyl)-2, 5-dimethoxy-4-nitro Benzene, 1-(1, l-dimethylethyl)-2-methoxy-4 methyl-5-nitro Benzaldehyde, 5- (1, l-dimethylethyl)-2-methyl-3-nitro Benzaldehyde, 2- (1, l-dimethylethyl)-4,5,6-trimethyl-3-nitro Benzene, 5-(l, l-dimethylethyl)-2-methoxy-l, 3-dinitro Benzene, 1-(1, l-dimethylethyl)-4-methoxy-2-methyl 3-5-dinitro Benzene, 2-bromo-5- (1, l-dimethylethyl)-4-methoxy-l,... 

Bromo-2-tert-butyl-4-nitro-benzene, AR70... 

Start by analyzing whether the bromo. nitro, or pentyl groups can be added to the appropriate disubstituted benzene with the required orientation. 

No Name Boiling poinl, C Melting point C n o "D Djo Picrate Sulfon amide Nitro derivative Bromo derivalive nitro benzene addition 3,5- Dmitro- benzoate Miscellaneous... 

No Name Melting point. C Boiling point, c d Df Picrate Sulfon amide Nitro derivative Bromo derivative nitro- benzene addition Dinilro ben zoate Miscellaneous... 

Name Melting poini c Boiling point c "d Dt" Picraie Sulfon amide Niiro derivative Bromo derivative 1 35 Tn nitro benzene addition com pound 3 5- Dinitro- ben zoale... 

The mono-, chloro-, bromo-, and iodo-benzenes are colourless liquids of peculiar odour. Di-chloro-, di-bromo-benzenes, tri- and hexa-chloro- and bromo-benzenes, are also known and mono-chloro-, C 6 H 4 C1(CH 3 ), and bromo-toluenes, together with di derivatives in the ortho, meta, and para modifications. The nitro-benzenes and toluenes are used as explosives. The following summary is taken from Dr A. Bemthsen s "Organic Chemistry" —... 

No Name Boiling point, C Melting point C "d Dr Picrate Sulfon amide Nitro denvativc Bromo denvative nitro benzene addition Miscellaneous... 

No Name Mdting point c Boiling point c "0 DJ Picrate Sulfon- amide Nitro- denvalive Bromo denvatrvc nitro benzene addition 35 Dinitro ben Miscellaneous... 

An extensive table of log k values for 32 phenols and substituted phenols (nitro, chloro, bromo, alkyl), benzene and substituted benzenes (alkyl, chloro, bromo), and naphthalene, anthracene, pyrene, and chrysene was generated by Bosch et al. [107]. Mobile phase compositions covered the entire 100% water to 100% acetonitrile range. No values were generated for logk values >2. Although these data were used to help generate a predictive retention scheme, the results are an excellent resource for use in method development. 

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