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| | Isophthalic dihydrazide Basic information |
| Product Name: | Isophthalic dihydrazide | | Synonyms: | 1,3-Bis(hydrazinocarbonyl)benzene;Isophthaloylbishydrazine;1,3-Benzenedicarboxylicacid, 1,3-dihydrazide;Isophthaloyl hydrazide;1,3-denzenedi carboxylic acid dihydrazide;5-Methylisophthalohydrazide;Benzene-1,3-dicarbohydrazide;ISOPHTHALIC DIHYDRAZIDE | | CAS: | 2760-98-7 | | MF: | C8H10N4O2 | | MW: | 194.19 | | EINECS: | 220-425-7 | | Product Categories: | Pharmaceutical intermediates;R00001 | | Mol File: | 2760-98-7.mol |  |
| | Isophthalic dihydrazide Chemical Properties |
| Melting point | 224°C | | density | 1.344±0.06 g/cm3(Predicted) | | vapor pressure | 0-0Pa at 20-25℃ | | storage temp. | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | | form | Solid:particulate/powder | | pka | 11.87±0.10(Predicted) | | color | White to Almost white | | InChI | InChI=1S/C8H10N4O2/c9-11-7(13)5-2-1-3-6(4-5)8(14)12-10/h1-4H,9-10H2,(H,11,13)(H,12,14) | | InChIKey | UTTHLMXOSUFZCQ-UHFFFAOYSA-N | | SMILES | C(NN)(C1C=C(C=CC=1)C(NN)=O)=O | | LogP | -1.4 at 20℃ and pH7.1 | | Surface tension | 74.4mN/m at 1g/L and 20℃ | | CAS DataBase Reference | 2760-98-7(CAS DataBase Reference) | | EPA Substance Registry System | Isophthalic acid dihydrazide (2760-98-7) |
| | Isophthalic dihydrazide Usage And Synthesis |
| Uses | Isophthalic dihydrazide serves as a precursor for synthesizing Schiff bases through condensation with substituted benzaldehydes, including 2-hydroxy-3-methoxybenzaldehyde, to evaluate antioxidant properties[6]. | | Synthesis | Isophthalic dihydrazide is prepared by the reaction of Dimethyl isophthalate and Hydrazine hydrate. The specific synthesis steps are as follows:
A mixture of dimethyl ester of isophthalic acid (2.22 gm) and hydrazine hydrate (98percent, 2 cc) in methanol was refluxed for 5 hours and the reaction mixture was allowed to cool to room temperature. Then, the cooled reaction mixture was poured on to ice cold water. The dihydrazide of isophthalic acid thus obtained was filtered and recrystallized from ethanol. [1] Yield: (85percent), M.P=241℃, (Scheme1). 1HNMR (400 MHz, CDCL3, ppm): 9.81 (s, 2H, -CO-NH-), 8.20 (s 1H ), 7.8(d, 2H, J=7.6 Hz), 7.5 (t, 1H, 7.2 Hz), 4.5 (s, 4H).
 | | References |
[1] Journal of the American Chemical Society, 2018,
[2] Bioorganic Chemistry, 2018, vol. 81, p. 389 - 395
[3] Pharmaceutical Chemistry Journal, 2001, vol. 35, # 12, p. 653 - 656
[4] Heterocyclic Communications, 2008, vol. 14, # 1-2, p. 101 - 105
[5] Organic and Biomolecular Chemistry, 2014, vol. 12, # 25, p. 4445 - 4453
[6]Khan, M., Raheel, M., Shah, S., Ibrahim, M., Asif, M., Salar, U., & Khan, K. M. (2023). Synthesis, Characterization, DPPH, Ferric Reducing, and Ferrous Ion- Chelating Activities of Isophthalate Schiff Bases. Letters in Drug Design & Discovery, 20(1), 31–39. https://doi.org/10.2174/1570180819666220429151008
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| | Isophthalic dihydrazide Preparation Products And Raw materials |
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