《Synthesis and biological evaluation of new curcumin analogs inhibiting osteoclastogenesis》 was published in Heterocycles in 2020. These research results belong to Sugawara, Aoi; Ohashi, Toshika; Ogawa, Satoshi; Matsumoto, Naomi; Nakanishi-Matsui, Mayumi; Tamura, Satoru; Kawano, Tomikazu. Safety of 2,5-Dibromothiophene The article mentions the following:
A series of curcumin analogs (1-3) were newly designed and synthesized for the development of therapeutic agents for osteoporosis. Among the synthesized compounds, 2,5-substituted conjugated thiophene derivative (1a) and the corresponding pyrazine derivative (1c) were shown to be potential leads for the development of anti-osteoclastogenesis agent.2,5-Dibromothiophene(cas: 3141-27-3Safety of 2,5-Dibromothiophene) was used in this study.
2,5-Dibromothiophene(cas: 3141-27-3) , is mainly used as pharmaceutical intermediate and synthesis intermediate. 2,5-Dibromothiophene may be used in the preparation of soluble α,ω-diformyl-a-oligothiophenes.Safety of 2,5-Dibromothiophene
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary