I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Stock No. | Size | Price ($) | Quantity | Availability |
---|---|---|---|---|
B20249-88 | 2.5g | 67.40 |
|
|
B20249-09 | 10g | 212.00 |
|
|
The synthesis of the thienopyranone scaffold began with the alkylation of methyl 4-bromo-3-hydroxythiophene-2-carboxylate with N-acetylmorpholine.
Guillermo A. Morales; Joseph R. Garlich; Jingdong Su; Xiaodong Peng; Jessica Newblom; Kevin Weber and Donald L. Durden. Synthesis and Cancer Stem Cell-Based Activity of Substituted 5-Morpholino-7H-thieno[3,2-b]pyran-7-ones Designed as Next Generation PI3K Inhibitors. J. Med. Chem. 2013, 56 (5), 1922-1939.