Methyl 2,4-dinitro-6- phenyI

Binapacryl. 3-Methyl-2-butenoic acid 2-(i-meth-ylpropyl)-4,6-dinitrophenyl ester 3-methylcrotonic acid 2-seC butyl-4,6-dinitrophenyi ester 2-sec-butyl-4,6-dinitro-phenyi 3,3-dimethylacrylate 2-sec-butyl-4,6-dinitrophenyl 3-methyl-2-butenoate 2 sec-butyl-4,6-dinilrophenyl 3-methylcrotonate 2 -see-butyl-4,6-dinitrophenyl senecioate 3,3-dimethylacrylic acid 2-sec-butyl-4,6-dinitrophenyl es. ter 4,6-dinitro-2-sec-butylphenyl P,P-dimethylacrylate 3-methyl-2-butenoic acid 2-sec-butyl-4,6-diniirophenyl ester dinoseb methacrylate senecioic aeid 2-sec-butyl-4,6-dinitrophenyl ester ENT 25793 HOE 2784 Acricid Am-box Endosan Morocide Niagara 9044. mol... 

C H,N,07 N-Nitto-N-methyl-N - [2.4.dinitro. phenyi]-hamstof IS II 411., N-Nitro.N -[4.6-dinitto-3-inethyl-phenyl]-hacnatoil 12 n 481. 

Nitration of indolizines often runs the risk of oxidation. The orientation of the substitution appears to depend on the experimental conditions nitration of 2-methyIindolizine in a mixture of nitric acid and sulfuric acid occurs at the 1-position (46JCS1075) in acetic anhydride at -70 °C, on the other hand, 2-methyl-3-nitroindolizine is formed (72JCS(P1)2954). The nitration of 2-phenylindolizine with nitric acid in aqueous sulfuric acid gave 2-(4-nitro-phenyI)indolizine (32a) and l-nitro-2-(4-nitrophenyI) indolizine (32b) together with 20% of an unidentified dinitro compound, possibly 3-nitro-2-(4-nitrophenyl)indoIizine (32c) (79JCS(P2)312). 

N-Nitro-N-methyl-N -[2.8-dinitro-4-mBthyl-phenyI].hamsto f 18II 539. 

Oxo.2.4-diphe I-tetrahydro.l.2.4-thio diazin-l-dioxyd H, 138 s. a. 27, 821. Dlbenzyldlnltromethan 6 II517. x-Dinitro-dibenzylmethan 6, 613. Bb-[5-nitro.2-methyl.phenyI]-methan 5, 615, II 518. 

Biz- [3-nitro.4-methyl. phenyl] -methan 5, 615,1 290. II 518. x.Dinitro-bla-r4-methy]-phenyI]-methan 5, 615,1 260. 

Dinitro-6-aceto -2-methyl-l-[3-acet o -phenyI]-benzimidazol 28, 382. 

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