Product Name :
2-(Trifluoroacetyl)thiophene (CAS 651-70-7)
Synonym :
Application :
2-(Trifluoroacetyl)thiophene is a CF3 acetate thiophene compound
CAS:
651-70-7
Purity:
≥95%
Molecular Weight:
180.15
Formula :
C6H3F3OS
Physical state:
Liquid
solubility :
Shipping Condition :
Store at 4° C
Melting point:
SMILES:
C1=CSC(=C1)C(=O)C(F)(F)F
References:
:Cloning and overexpression of the Exiguobacterium sp. F42 gene encoding a new short chain dehydrogenase, which catalyzes the stereoselective reduction of ethyl 3-oxo-3-(2-thienyl)propanoate to ethyl (S)-3-hydroxy-3-(2-thienyl)propanoate.8-Bromoquinazoline-2,4-diol site | Wada, M.1-Bromo-2-fluorobenzene supplier , et al. 2004. Biosci Biotechnol Biochem. 68: 1481-8. PMID: 15277752Classification structure-activity relationship (CSAR) studies for prediction of genotoxicity of thiophene derivatives. | Du, H., et al. 2008. Toxicol Lett. 177: 10-9. PMID: 182435953D QSAR of aminophenyl benzamide derivatives as histone deacetylase inhibitors.PMID:33666048 | Mahipal, ., et al. 2010. Med Chem. 6: 277-85. PMID: 20977417Synthesis of pentafluorinated beta -hydroxy ketones. | Zhang, P. and Wolf, C. 2012. J Org Chem. 77: 8840-4. PMID: 22992005Precursor-directed combinatorial biosynthesis of cephalosporin analogue by endolithic actinobacterium Streptomyces sp. AL51 by utilizing thiophene derivative. | Bhattacharjee, K., et al. 2018. 3 Biotech. 8: 31. PMID: 29291144Reaction of indoles with aromatic fluoromethyl ketones: an efficient synthesis of trifluoromethyl(indolyl)phenylmethanols using K2CO3/n-Bu4PBr in water. | Pillaiyar, T., et al. 2020. Beilstein J Org Chem. 16: 778-790. PMID: 32395181Purification and characterization of fluorinated ketone reductase from Geotrichum candidum NBRC 5767 | Cao, C., Fukae, T., Yamamoto, T., Kanamaru, S., & Matsuda, T. 2013. Biochemical engineering journal. 76: 13-16.2-(Trifluoroacetyl) thiophene as an electrolyte additive for high-voltage lithium-ion batteries using LiCoO2 cathode. | Sun, Y., Huang, J., Xiang, H., Liang, X., Feng, Y., & Yu, Y. 2020. Journal of Materials Science & Technology. 55: 198-202.