thiotetronic acid

CCCCC/C=C\C/C=C\CCCCCCCC(=O)C1=C(O)CSC1=O
Reaction #5358
4-hydroxy-3-[(Z,Z)-1-oxo-9,12-octadecadienyl]-2(5H)-thiophenone
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCC/C=C\CCCCCCCC(=O)C1=C(O)CSC1=O
Reaction #5359
4-hydroxy-3-[(Z)-1-oxo-9-octadecenyl]-2(5H)-thiophenone
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCC/C=C\CCCCCCCC(=O)C1=C(O)CSC1=O
Reaction #5360
4-hydroxy-3-[(Z)-1-oxo-9-tetradecenyl]-2(5H)-thiophenone
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCCCOc1ccc(Cl)cc1)C1=C(O)CSC1=O
Reaction #5361
4-hydroxy-3-[5-(4-chlorophenoxy)-1-oxopentyl]-2(5H)-thiophenone
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)C1=C(O)CSC1=O
Reaction #5362
4-hydroxy-3-[(Z,Z,Z)-1-oxo-6,9,12-octadecatrienyl]-2(5H)-thiophenone
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCC/C=C\CCCCC(=O)C1=C(O)CSC1=O
Reaction #5363
4-hydroxy-3-[(Z)-1-oxo-6-octadecenyl]-2(5H)-thiophenone
Ausbeute 21.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #65580
3-(3-cyclododecyl-1-oxopropyl)-4-hydroxy-2(5H)-thiophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(CCCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #65586
white solid
Ausbeute 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(COC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #65587
3-(2-cyclododecyloxy-1-oxoethyl)-4-hydroxy-2(5H)-thiophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(CCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #216711
3-(3-cyclododecyl-1-oxopropyl)-4-hydroxy-2(5H)-thiophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C(CCCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #216717
white solid
Ausbeute 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C(COC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #216720
3-(2-cyclododecyloxyl-1-oxoethyl)-4-hydroxy-2(5H)-thiophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CSc1ccc(CC2=C(O)CSC2=O)cc1
Reaction #1063248
solid
Ausbeute 26.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
CSc1ccc(CC2=C(O)CSC2=O)cc1
Reaction #1844398
solid
Ausbeute 26.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_08
O=C(CCCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #2467548
white solid
Ausbeute 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_11
O=C(COC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #2467552
3-(2-cyclododecyloxy-1-oxoethyl)-4-hydroxy-2(5H)-thiophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_11