(methyldisulfanyl)methane

CSc1ccc(OCc2c(-c3ccccc3)noc2C)nc1
Reaction #170542
title compound
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cccc2sc(SC)nc12
Reaction #173084
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(-c2ccc(C(F)(F)F)cc2)nc1F
Reaction #177797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCc1nc(NC(=O)OC(C)(C)C)sc1SC
Reaction #179390
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1cc(C=O)cc(OCc2ccccc2)c1O
Reaction #180655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1cccc2c(-c3ccnc(NC4CCCC4)n3)c(CC(C)C)nn12
Reaction #182285
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1c(C(=O)O)ccc(Br)c1Cl
Reaction #189066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCN(CCC)C1Cc2ccc(SC)cc2C1
Reaction #195514
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(cc1OC)C(CCO)(SC)C(=O)N2
Reaction #198877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1cccc(C)c1C1=NOCC1
Reaction #200395
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C(=O)O)s1
Reaction #208282
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(Br)c(CN2C(=O)OC(c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2C)c1
Reaction #209292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(C)c(F)c1
Reaction #210890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1c(F)cccc1Cl
Reaction #211084
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(F)(F)F)cc(SC)c1C(=O)O
Reaction #211785
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1sc(C)c(Br)c1C
Reaction #214958
3-bromo-2,4-dimethyl-5-(methylthio)thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CSc1cc2ccccc2n1Cc1ccccc1
Reaction #216015
N-benzyl-2-(methylthio)indole
المردود 100.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CSC(C(=O)O)C(C)(C)c1ccccc1
Reaction #221028
3-methyl-2-(methylsulfanyl)-3-phenylbutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CSc1ccc(Oc2ccc(Br)cc2)cc1O
Reaction #222161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(C)c(F)c1
Reaction #223969
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
السابقالصفحة 2التالي