thioglycolic acid

Cc1ccc(S(=O)(=O)c2ccc(CC(O)=S)cc2)cc1
Reaction #2488
4-(4-methylphenylsulfonyl)phenylthio acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC(=S)CCc1cccc(Br)c1
Reaction #50550
3-bromophenylmethylthioacetic acid
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C1CSC(C(=O)O)O1
Reaction #52556
5-oxo-1,3-oxathiolane-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCC(O)CCN1C(=O)CSC1CCCc1ccc(C(=O)OCC)cc1
Reaction #56482
title compound
Ausbeute 31.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56484
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C=CC(=O)OCCO.C=CC(=O)[O-]
Reaction #62792
Hydroxyethylacrylate Acrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COc1cc(C(C#N)c2ccc(Cl)cc2)ccc1-n1ncc(=O)[nH]c1=O
Reaction #63833
intermediate 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(=O)S[C@H]1C[C@@H](C(=O)N2CCN(CCOC(=O)OCc3ccc([N+](=O)[O-])cc3)CC2)N(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65622
title compound
Ausbeute 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)[C@H](CC(C)C)N1C(=O)CSC1c1ccc(Cl)cc1
Reaction #78918
4-Methyl-2-(S)-[2-(RS)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic Acid Methyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(SCC(=O)O)CCCO1
Reaction #83835
26
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cccc(NCC(F)Cn2c3ccc(Br)cc3c3cc(Br)ccc32)c1
Reaction #90421
N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-3-methoxyaniline
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cccc(NCC(F)Cn2c3ccc(Br)cc3c3cc(Br)ccc32)c1
Reaction #90455
N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-3-methoxyaniline
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(CCCNCCn3ccc4ccccc4c3=O)ccc21
Reaction #156170
title compound
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)CSc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #161234
2-(2,4-dinitrophenylthio)-acetic acid
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)n2cc(C)c3c(-c4nc5c(c(N6CCN[C@H](C)C6)n4)CN(c4cc(C(C)C)nn4C)CC5)cccc32)cc1
Reaction #167992
(R)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methylpiperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CCc1ccc(NCc2cccc(-c3c(C)cc(OCC4(O)CCS(=O)CC4)cc3C)c2)cc1F
Reaction #172965
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(SCC(=O)O)c1ccc(-c2ccccc2F)cc1
Reaction #184379
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CSc1nc(C(=O)NCc2ccc(F)cc2)c(O)c2ncccc12
Reaction #198056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(=O)OCC1OC(=O)CS1
Reaction #203253
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)c1ccc(N2CCC(Nc3ccccn3)C2)cc1
Reaction #207637
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Seite 1Weiter