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2-Nitrotoluene is hydrogenated to give o-toluidine. [2] The conversion of o-toluidine to the diazonium salt gives access to the 2-bromo, 2-cyano-, and 2-chlorotoluene derivatives. [3] [4] [5] N-acetylation is also demonstrated. [6]
4-Nitrotoluene or para-nitrotoluene is an organic compound with the formula CH 3 C 6 H 4 NO 2. It is a pale yellow solid. It is one of three isomers of nitrotoluene.
2-Nitrotoluene or ortho-nitrotoluene is an organic compound with the formula CH 3 C 6 H 4 NO 2. It is pale yellow liquid that crystallizes in two forms, called α (−9.27 °C) and β (−3.17 °C). It is mainly a precursor to o-toluidine, which is an intermediate in the production of various dyes. [4]
2-Nitrobenzoic acid is prepared by oxidation of 2-nitrotoluene. 3-Nitrobenzoic acid is a precursor to 3-aminobenzoic acid, which in turn is used to prepare some dyes. It can be prepared by nitration of benzoic acid. It also can be prepared by treating benzaldehyde under nitration conditions, a process that initially converts the aldehyde to the ...
The molecular formula C 7 H 7 NO 2 (molar mass: 137.14 g/mol) may refer to: Aminobenzoic acids 2-Aminobenzoic acid (o-aminobenzoic acid, anthranilic acid) 3-Aminobenzoic acid (m-aminobenzoic acid) 4-Aminobenzoic acid (p-aminobenzoic acid, PABA) Mononitrotoluenes. 2-Nitrotoluene; 3-Nitrotoluene; 4-Nitrotoluene; Salicylaldoxime; Salicylamide ...
The most common one is 2,4-dinitrotoluene. The nitration of toluene gives sequentially mononitrotoluene, DNT, and finally TNT. 2,4-DNT is the principal product from dinitration, the other main product being about 30% 1,3-DN2-T. The nitration of 4-nitrotoluene gives 2,4-DNT. [5]
2,4-Dinitrotoluene; M. Mononitrotoluene; N. 2-Nitrotoluene; 3-Nitrotoluene; 4-Nitrotoluene This page was last edited on 30 January 2024, at 19:32 ...
Thus, adsorption of the TNT decomposition product 2,4-diamino-6-nitrotoluene (2,4-DANT) was greater than that for 4-amino-2,6-dinitrotoluene (4-ADNT), which was greater than that for TNT. [41] Lower adsorption coefficients for 2,6-DNT compared to 2,4-DNT can be attributed to the steric hindrance of the NO 2 group in the ortho position.