The author of 《Synthesis of nonembryonic synseeds in Hemidesmus indicus R. Br.: short term conservation, evaluation of phytochemicals and genetic fidelity of the regenerants》 were Yadav, V.; Shahzad, A.; Ahmad, Z.; Sharma, S.; Parveen, S.. And the article was published in Plant Cell, Tissue and Organ Culture in 2019. Computed Properties of C8H8O3 The author mentioned the following in the article:
Non-embryogenic, synthetic seeds were formed by encapsulating the nodal segments (NS) of Hemidesmus indicus R. Br. in calcium alginate hydrogel comprising of MS basal medium for short-term conservation. A 3% sodium aliginate (SA) with 100 mM CaCl2 was found most suitable for the preparation of isodiametrical beads. Highest shoot regrowth (84.50 ± 0.35%) was recorded when the gelling matrix, i.e. 3% SA in Murashige and Skoog (MS) basal medium was supplemented with 5.0μM 6-benzyladenine (BA) + 0.5μM indole-3-butyric acid (IBA) and inoculated onto the nutrient medium comprised of MS + 5.0μM BA gave 5.53 ± 0.096 shoots/encapsulated NS. Rooting in microshoots was obtained on the half strength liquid MS + 0.1μM IBA. Plantlets achieved from preserved synthetic seeds were acclimatized and relocated in the natural condition successfully with the immortality rate of 89.3%. During the days of acclimatization, the obtained plants were subjected for the assessment of their pigment content and biochem. assay. The results obtained clearly exhibited the enhancement in the pigment content as the acclimatization period increases. A significant rise and fall in Superoxide dismutase (SOD), Catalase (CAT), Glutathione reductase (GR) and Ascorbate peroxidase (APX) were evident, suggesting their preventive role against the several environmental stresses during the acclimatization of the plant. In the part of experimental materials, we found many familiar compounds, such as 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Computed Properties of C8H8O3)
2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Computed Properties of C8H8O3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem