ethyl 2-sulfanylacetate

CCOC(=O)c1sc(-c2ccc(C(F)(F)F)cc2)cc1C
Reaction #9734
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=S)CCc1ccc([N+](=O)[O-])cc1
Reaction #55091
stated product
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #55459
carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=S)CCc1ccc([N+](=O)[O-])cc1
Reaction #56460
stated product
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=O)c1sc2ncccc2c1N
Reaction #58696
title compound
収率 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)CSCC(=O)Nc1c(C(C)C)cccc1C(C)C
Reaction #65042
N-(2,6-diisopropylphenyl)-2-(ethoxycarbonylmethylthio)acetamide
収率 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)c1sc2cc([N+](=O)[O-])ccc2c1N
Reaction #72075
title compound
収率 32.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cc2c(nc(COC)n2C)s1
Reaction #78658
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)CSCCCC(O)c1ccco1
Reaction #94691
4-(carbethoxymethylthio)-1-(2-furyl)-1-butanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCCCCCc1c(C(=O)OCC)sc2ccsc12
Reaction #171142
compound 61
収率 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1cc2c(s1)CCOc1ccccc1-2
Reaction #171801
4,5-dihydro-6-oxa-3-thia-benzo[e]azulene-2-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1CCC(N(C(=O)Nc2ncc(SCC(=O)O)s2)C2CCC2)CC1
Reaction #174023
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CSc1cc(C)nc(N)n1
Reaction #188636
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC1(CC)CN(c2ccccc2)c2cc(SCC(=O)OCC)c(OCC(=O)O)cc2S(=O)(=O)C1
Reaction #188867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CSCc1cc2cccc([N+](=O)[O-])c2o1
Reaction #192003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CSCC1C(C(=O)OCC)C1C(NC(=O)OC(C)(C)C)C(=O)OCC
Reaction #196865
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CSC(C)(C)C(=O)CC
Reaction #217553
ethyl[(1,1-dimethyl-2-oxobutyl)thio]acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=CCOC(=O)CCCSCC(=O)OCC
Reaction #229859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)CSC1=C(C(=O)OC)CN(C(=O)c2ccccc2)CC1
Reaction #235800
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)CSCc1ccc(C(F)(F)F)cc1
Reaction #247871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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