2904209090 derivatives containing only nitro or only nitroso groups。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%
2.
The influence of the nitro-group upon side-chain reactivity. Part IV. The inhibition of α-proton extraction from 4-nitrobenzyl chloride by the steric effect of methyl groups in the 3- and 5-positions D. M. Doleib,Y. Iskander J. Chem. Soc. B 1967 1154
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Research progress on photocatalytic reduction of CO2 based on LDH materials Zhe-xu Bi,Rui-tang Guo,Xing Hu,Juan Wang,Xin Chen,Wei-guo Pan Nanoscale 2022 14 3367
7.
The influence of the nitro-group upon side-chain reactivity. Part VI. The d-orbital resonance stabilisation of α-bromo- and α-iodo-4-nitrobenzyl anions, retarding their α-elimination to 4-nitrophenylcarbene A. A. Abdallah,Y. Iskander,Y. Riad J. Chem. Soc. B 1969 1178
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Notes G. M. Badger,P. Cheuychit,W. H. F. Sasse,T. C. W. Mak,J. Trotter,A. R. Battersby,D. J. Le Count,W. P. Griffith,Z. S. Krzeminski,S. J. Angyal,B. H. M. Billinge,B. G. Gowenlock,G. M. Brooke,J. Burdon,J. C. Tatlow,S. J. Gregg,R. F. S. Tyson,W. Carruthers,J. R. Plimmer,D. Lavie,Y. Shvo,O. R. Gottlieb,R. B. Desai,M. L. Khorana,A. Holland,Leo A. Pohoryles,Izhar Gat,Shalom Sarel,J. D. Loudon,A. D. B. Sloan,Peter Bladon,Thomas Sleigh,W. Hewertson,R. A. Shaw,B. C. Smith,J. Chatt,B. L. Shaw,A. A. Williams,M. Halmann,L. Kugel,G. W. Kirby,G. Shaw,A. Yeadon,H. J. Emeléus,G. L. Hurst,John G. Carey,Ian T. Millar,Stanley S. Brown,Roy Wade,D. H. Brown,D. J. Alner J. Chem. Soc. 1962 3241
9.
Nitrophenylcarbenes. Part III. Kinetics of the decomposition of 4-nitrobenzyl chloride and dimethyl-4-nitrobenzylsulphonium ion in sodium hydroxide. A reinvestigation G. L. Closs,S. H. Goh J. Chem. Soc. Perkin Trans. 2 1972 1473
10.
Nitrophenylcarbenes. Part III. Kinetics of the decomposition of 4-nitrobenzyl chloride and dimethyl-4-nitrobenzylsulphonium ion in sodium hydroxide. A reinvestigation G. L. Closs,S. H. Goh J. Chem. Soc. Perkin Trans. 2 1972 1473