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Purchase CAS:406-15-5 | Carbonic acid bis(2-fluoroethyl) ester,view related peer-reviewed papers,technical documents,similar products,MSDS & more.Thiophene derivatives are a class of organic compounds that have been the subject of intensive study due to their potential biological activities . They play a vital role for medicinal chemists to improve advanced compounds with a variety of biological effects ....
Thiophene derivatives are a class of organic compounds that have been the subject of intensive study due to their potential biological activities. They play a vital role for medicinal chemists to improve advanced compounds with a variety of biological effects.
Thiophene derivatives can be synthesized through various methods, including the Gewald reaction, Paal–Knorr synthesis, Fiesselmann synthesis, and Hinsberg synthesis. The specific synthesis route for “5-Methyl-3-[(2-methylpropan-2-yl)oxycarbonylamino]thiophene-2-carboxylic acid” is not available in the current literature.
Thiophene derivatives are known to undergo a variety of chemical reactions, including electrophilic substitution, nucleophilic substitution, and coupling reactions. The specific chemical reactions involving “5-Methyl-3-[(2-methylpropan-2-yl)oxycarbonylamino]thiophene-2-carboxylic acid” are not available in the current literature.
The future directions in the field of thiophene derivatives research could involve the development of new synthetic methods, the discovery of novel thiophene-based drugs, and the exploration of their biological activities.
Product Name: | Carbonic acid bis(2-fluoroethyl) ester |
Synonyms: | Carbonic acid bis(2-fluoroethyl) ester;IL-885;Ethanol, 2-fluoro-, 1,1'-carbonate;Bis(2-fluoroethyl) carbonate |
CAS: | 406-15-5 |
MF: | C5H8F2O3 |
MW: | 154.11 |
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Mol File: | 406-15-5.mol |
Carbonic acid bis(2-fluoroethyl) ester Chemical Properties |
Boiling point | 183.95°C (rough estimate) |