Busqueda de Subestructura

C1CS1

C1CSC2(S1)SCC(CSCC1CSC3(SCCS3)S1)S2
Reaction #43522
2,2′-[thiobis(methylene)]bis-1,4,6,9-tetrathiaspiro[4.4]nonane
Rendimiento 4.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(S)CSCc1cc(CO)cc(CO)c1
Reaction #86285
(5-((2-mercapto-2-methylpropylthio)methyl)-1,3-phenylene)dimethanol
Rendimiento 59.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(S)CCC(=O)O
Reaction #165735
product 7
Rendimiento 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2ccccc2sc2cc(OCC(S)CCl)cc(O)c12
Reaction #170285
title compound
Rendimiento 71.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c(=O)c3c(O)cc(OCC(S)CCl)cc3oc12
Reaction #170286
title compound
Rendimiento 90.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2c(O)cc(OCC3CS3)cc2oc2ccc3ccccc3c12
Reaction #170287
11-hydroxy-9-(thiiran-2-ylmethoxy)-12H-benzo[a]xanthen-12-one
Rendimiento 43.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cc3ccccc3cc2oc2cc(OCC3CS3)cc(O)c12
Reaction #170290
title compound
Rendimiento 20.8%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2CS2)cc1
Reaction #197960
DOI: 10.1039/C8SC04228D
C=C(C)C(=O)OCC1CS1
Reaction #215333
2,3-epithiopropyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC1=CCSC1
Reaction #232094
DOI: 10.1039/C8SC04228D
COCC1(COC)CS1
Reaction #286753
DOI: 10.1039/C8SC04228D
COC(=O)Cc1ccc(Oc2ccc(S(=O)(=O)CC(C)C3CS3)cc2)cc1
Reaction #288328
DOI: 10.1039/C8SC04228D
SCCC1c2ccccc2-c2ccccc21
Reaction #293706
DOI: 10.1039/C8SC04228D
O=S(=O)([O-])C(F)(F)F.OCc1cc[n+](CCS)cc1
Reaction #323231
4-Hydroxymethyl-1-(2-mercaptoethyl)pyridinium trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)[O-].Cc1cccc[n+]1CCS
Reaction #323232
title compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc[n+](CCS)cc1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #323233
title compound
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)[O-].CSc1cc[n+](CCS)cc1
Reaction #323234
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc[n+](CCS)c1.[Cl-]
Reaction #323235
3-Methylthio-1-(2-mercaptoethyl)pyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)[O-].Cc1cccc(C)[n+]1CCS
Reaction #323236
impure title compound
Rendimiento 19.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(COc2cccc3c2CC2SC2C3)cc1
Reaction #354745
6,7-epithio-5,6,7,8-tetrahydronaphthyl benzyl ether
DOI: 10.6084/m9.figshare.5104873.v1
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