trifluoromethanesulfonic acid

CCCc1cc(=O)oc2cc(O)cc(O)c12
Reaction #1281
coumarin
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1[C@@H](N2C(=O)c3ccccc3C2=O)Cc2ccccc2C2CCC=CN12
Reaction #3771
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NCCC1S.O=S(=O)(O)C(F)(F)F
Reaction #5214
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCC[C@H](CC(=O)OC)OCc1ccccc1
Reaction #5717
methyl (R)-3-(benzyloxy)-tetradecanoate
Ausbeute 112.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Oc1ccc(C(c2ccccc2)(c2ccc(O)cc2)C(F)(F)F)cc1
Reaction #6292
1,1-bis(4-hydroxyphenyl)-1-phenyl-2,2,2-trifluoroethane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCc4cccc(CO[Si](C)(C)C(C)(C)C)c4)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6392
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CC1OC
Reaction #6393
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6394
title compounds
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6395
title compounds
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #6396
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=C(CC)OC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6397
title compounds
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CC1OC
Reaction #6399
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CC1OC
Reaction #6400
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)[C@H](C)Nc1ccc(F)c(F)c1F
Reaction #8524
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCc1cc(C(=O)CC)cc(CCC)c1O
Reaction #9346
phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCc1cc(C(=O)CC)c(F)c(CCC)c1O
Reaction #9348
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(N1CC2CC(C1)c1cc([N+](=O)[O-])ccc12)C(F)(F)F
Reaction #10181
product
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=C(C)C(=O)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C
Reaction #44314
nonamethyl-1-methacryloyloxy-tetrasiloxane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1CCC(=C2c3ccc(Cl)cc3C(=O)Cc3cccnc32)CC1
Reaction #49692
8-chloro-5,11-dihydro-11-(1-methyl-4-piperidinylidene)-6H-benzo[5,6]cyclohepta-[1,2-b]pyridin-6-one
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
C=CCOC[C@H](NC(=O)C(Cc1ccccc1)N1C(=O)c2ccccc2C1=O)C(=O)OC
Reaction #49966
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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