مشارك في 495 تفاعل

C(CS)O

COC(=O)c1ccc2c(c1)C(SCCO)c1ccccc1CO2
Reaction #5139
methyl 11-(2-hydroxyethyl)thio-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)N1CCCC1c1cc2[nH]c(-c3ccccn3)nc2cc1Oc1ccc(SCCO)nc1
Reaction #41695
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OCCSc1cc(Cl)nnc1Cl
Reaction #43430
2-[(3,6-Dichloro-4 pyridazinyl)thio]ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccc(SCCO)c([N+](=O)[O-])c1
Reaction #49954
2-[2,4-dinitrophenylsulfanyl]ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
C=C.O=C(Cn1ccnc1)c1ccc2ccccc2c1
Reaction #54821
1-[2-naphthoylmethyl]imidazole ethylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1(c2ccccc2)OC(CC(SCCO)c2ccsc2)=CC1=O
Reaction #78306
5-[2-[(2-hydroxyethyl)thio]-2-(3-thienyl)ethyl]-2-methyl-2-phenylfuran-3(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(c2ccc(F)cc2)OC(CC(SCCO)c2ccsc2)=CC1=O
Reaction #78307
2-(4-fluorophenyl)-5-[2-[(2-hydroxyethyl)thio]-2-(3-thienyl)ethyl]-2-methylfuran-3(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(CCCSCCO)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80327
title compound
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(CSCCO)NCCCOc1cc(CN2CCCCC2)ccn1
Reaction #80373
title compound
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(CCCCCSCCO)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80384
title compound
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #92673
liquid
المردود 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #92674
liquid
المردود 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1c2c(O)cccc2C(SCCO)c2cccc(O)c21
Reaction #173850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2nc(CSCCO)nc3cc(OC)c(OC)cc23)cc1OC
Reaction #173943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(O)C(=O)OCc2c1cc1n(c2=O)Cc2c-1nc1ccccc1c2CC[Si](C)(C)CSCCO
Reaction #174700
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCSCCc1ccncc1
Reaction #176549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc(SCCO)c([N+](=O)[O-])c1
Reaction #176779
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)N1c2ccc(OC)nc2C(c2ncc(SCCO)c(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)n2)CC1(N)CC
Reaction #177036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nc(Cl)c(Cl)c1SCCO
Reaction #177590
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCSCCO
Reaction #180838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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