tetrafluorophthalic anhydride

CCN1C(=O)NC(=O)C(C)(N2C(=O)c3c(F)c(F)c(F)c(F)c3C2=O)C1=O
Reaction #187440
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(N2C(=O)c3c(F)c(F)c(F)c(F)c3C2=O)C(=O)NC(=O)N(c2ccccc2)C1=O
Reaction #195972
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #201272
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(F)c(F)c(F)c1F
Reaction #235429
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #292885
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #347136
3,4,5,6-tetrafluorophthalic acid-monomethyl ester
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)c1cc(F)c(F)c(F)c1F
Reaction #347140
3,4,5,6-tetrafluorobenzoic acid methyl ester
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COc1c(F)c(F)cc(C(=O)O)c1F
Reaction #347145
3-methoxy-2,4,5-trifluorobenzoic acid
Yield 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #352842
3,4,5,6-tetrafluorophthalic acid-monomethyl ester
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COC(=O)c1cc(F)c(F)c(F)c1F
Reaction #352846
3,4,5,6-tetrafluorobenzoic acid methyl ester
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COc1c(F)c(F)cc(C(=O)O)c1F
Reaction #352851
3-methoxy-2,4,5-trifluorobenzoic acid
Yield 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCOc1c(F)c(F)cc(C(=O)O)c1F
Reaction #463206
3-ethoxy-2,4,5-trifluorobenzoic acid
Yield 77.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
O=C(O)c1cc(F)c(F)c(OCC(F)(F)F)c1F
Reaction #463207
3-trifluoroethoxy-2,4,5-trifluorobenzoic acid
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
O=C(O)c1cc(OCc2ccc(F)cc2)c(F)c(F)c1F
Reaction #463208
(4-fluorobenzyloxy) trifluorobenzoic acid
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
O=C(O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #709443
tetrafluorophthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
O=C(O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #709444
tetrafluorophthalic acid
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
O=C(O)c1c(F)c(F)c(F)c(F)c1C(=O)O
Reaction #709445
tetrafluorophthalic acid
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
O=C1c2c(F)c(F)c(F)c(F)c2C(=O)N1c1ccc(F)cc1F
Reaction #787368
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CN1C(=O)NC(=O)C(C)(N2C(=O)c3c(F)c(F)c(F)c(F)c3C2=O)C1=O
Reaction #1026527
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
NNC(=O)c1c(F)c(F)c(F)c(F)c1C(=O)NN
Reaction #1052049
Compound 43
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
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