2,2,3,3,3-pentafluoropropanol

Cc1ccc(S(=O)(=O)OCC(F)(F)C(F)(F)F)cc1
Reaction #205054
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)c1ccc(OCC(F)(F)C(F)(F)F)c(C(=O)O)c1
Reaction #245788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(S(=O)(=O)OCC(F)(F)C(F)(F)F)cc1
Reaction #250744
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
FC(F)(F)c1ccc2oc(-c3ccncc3OCC(F)(F)C(F)(F)F)nc2c1
Reaction #258303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)C(CSC(c1ccccc1)(c1ccccc1)c1ccccc1)NCC(F)(F)C(F)(F)F
Reaction #407069
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1c(OCC(F)(F)C(F)(F)F)cc[n+]([O-])c1C
Reaction #440185
2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1ccc([N+](=O)[O-])cc1COCC(F)(F)C(F)(F)F
Reaction #460543
3-(2,2,3,3,3-pentafluoropropoxy)methyl-4-methyl-1-nitrobenzene
المردود 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
Cc1c(OCC(F)(F)C(F)(F)F)cc[n+]([O-])c1C
Reaction #465939
2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
C=C(C(F)(F)F)C(F)(F)OCC(F)(F)C(F)(F)F
Reaction #579455
CH2═C(CF3)CF2OCH2CF2CF3
المردود 116.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(Nc1cccc(C(=O)Nc2ccc(C(F)(F)F)cc2C(F)(F)F)c1)OCC(F)(F)C(F)(F)F
Reaction #598941
title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
O=C(NN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)C[C@@H](O)C(=O)OCC(F)(F)C(F)(F)F)c1cc(-c2ccccc2F)no1
Reaction #628691
title compound
المردود 12.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COc1cc(C(=O)NN(Cc2ccc(-c3cc(Cl)ccc3F)cc2)C[C@@H](O)C(=O)OCC(F)(F)C(F)(F)F)on1
Reaction #628700
title compound
المردود 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C(NN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)C[C@@H](O)C(=O)OCC(F)(F)C(F)(F)F)c1nn(-c2ccccc2)c(=O)[nH]1
Reaction #628713
title compound
المردود 8.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
N#Cc1cccc(OCC(F)(F)C(F)(F)F)c1C#N
Reaction #654026
intended compound
المردود 95.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
Cc1c[n+]([O-])cc(C)c1OCC(F)(F)C(F)(F)F
Reaction #709339
3.5-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide
المردود 80.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
COC(=O)c1ccc(OCC(F)(F)C(F)(F)F)nc1
Reaction #710679
title compound
المردود 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COC(=O)c1ccc(OCC(F)(F)C(F)(F)F)nc1
Reaction #710683
title compound
المردود 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=C(O)c1ccc(Br)c(OCC(F)(F)C(F)(F)F)n1
Reaction #712129
title compound
المردود 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=C(O)c1ccc(Br)c(OCC(F)(F)C(F)(F)F)n1
Reaction #719538
title compound
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=C(O)[C@H](CSC(c1ccccc1)(c1ccccc1)c1ccccc1)NCC(F)(F)C(F)(F)F
Reaction #730087
2(R)-(2,2,3,3,3-pentafluoropropylamino)-3-tritylsulfanylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
الصفحة 1التالي