It forms yellow plates from AcOH and needles from EtOH [Slotta & Szyszke Chem Ber 68 184 1935]. With diazomethane, 5-nitro-3,4-dimethoxyacetophenone is formed [Brady & Manjunath J Chem Soc 125 1067 1924]. The methyl ether crystallises from EtOAc or AcOH, m 88o, 90-91o, and the phenylhydrazone has m 108-110o (from aqueous EtOH). [Finger & Schott J Prakt Chem [2] 115 288 1927.] The oxime has m 216o (from EtOH or AcOH), and the oxime acetate has m 147o (from aqueous EtOH) [Vogel Monatsh Chem 20 384 1899, Brady & Dunn J Chem Soc 107 1861 1915]. [Beilstein 8 III 2064.]
[1] Journal of Physical Organic Chemistry, 2000, vol. 13, # 9, p. 511 - 517
[2] Journal of Medicinal Chemistry, 2010, vol. 53, # 8, p. 3396 - 3411
[3] Tetrahedron Letters, 2006, vol. 47, # 15, p. 2507 - 2509
[4] Synthetic Communications, 2008, vol. 38, # 11, p. 1745 - 1752
[5] Tetrahedron, 1992, vol. 48, # 10, p. 1895 - 1910