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Thiophene is a heterocyclic compound with the formula C 4 H 4 S. Consisting of a planar five-membered ring, it is aromatic as indicated by its extensive substitution ...
Thiofentanyl is an opioid analgesic that is an analogue of fentanyl.. Thiofentanyl was sold briefly on the black market in the early 1980s, before the introduction of the Federal Analog Act which for the first time attempted to control entire families of drugs based on their structural similarity rather than scheduling each drug individually as they appeared. [1]
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Thiophene-2-carboxylic acid is an organic compound with the formula SC 4 H 3 CO 2 H. It is one of two mono carboxylic acids of thiophene , the other being thiophene-3-carboxylic acid. [ 1 ] Copper(I) thiophene-2-carboxylate is a catalyst for Ullmann coupling reactions .
Both unsubstituted and substituted tetrahydrothiophenes are reported to occur in nature. For example, tetrahydrothiophene occurs as a volatile from Eruca sativa Mill. . (salad rocket) [5] while monocyclic substituted tetrahydrothiophenes have been isolated from Allium fistulosum 'Kujou', [6] Allium sativum (garlic), [7] Allium cepa (onion), [8] Allium schoenoprasum (chives), [9] and Salacia ...
Thieno[3,2-b]thiophene. In organic chemistry, thienothiophene is any of several compounds consisting of two fused thiophene rings. They have the molecular formula C 6 H 4 S 2. Three constitutional isomers have been synthesized: thieno[3,2-b]thiophene, thieno[2,3-b]thiophene, and thieno[3,4-b]thiophene. The other isomer features S(IV) and is ...
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