Recherche de Sous-structure

COC(=O)CS

CCOC(=O)Cc1nc2ccc(Br)cc2s1
Reaction #10482
6-bromo-benzothiazol-2-yl-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1nc2ccc(Br)cc2s1
Reaction #10497
(6-bromo-benzothiazol-2-yl)-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Sc2cc(Cl)ccc2OC1=O
Reaction #11787
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)(C(=O)O)S(=O)(=O)c1ccccc1
Reaction #52175
2-ethyl-2-(phenylsulfonyl)Butanoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Sc1ccc(C)cc1)Sc1ccc(C)cc1
Reaction #56393
Ethyl 2,2-bis(4-methylthiophenoxy)acetate
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Sc1ccncc1Br
Reaction #74049
ethyl 2-(3-bromopyridin-4-ylthio)-2-methylpropanoate
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Sc1ccncc1-c1ccc(C#N)cc1
Reaction #74050
ethyl 2-(3-(4-cyanophenyl)pyridin-4-ylthio)-2-methylpropanoate
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)c1cnc2c(F)cccc2c1O
Reaction #159822
4-hydroxy-3-phenylsulfonyl-8-fluoroquinoline
Rendement 3.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CSCc1ccc(OC)c([N+](=O)[O-])n1
Reaction #159842
Methyl 2-((5-methoxy-6-nitropyridin-2-yl)methylthio)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSCC(=O)O)nc1[N+](=O)[O-]
Reaction #159843
2-((5-methoxy-6-nitropyridin-2-yl)methylthio)acetic acid
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CS(=O)Cc1ccc(OC)c([N+](=O)[O-])n1
Reaction #159844
titled compound
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CS(=N)(=O)c1ccccc1
Reaction #177867
DOI: 10.1039/C8SC04228D
CCCCC(Cc1ccc(OCCN(CC)CC)cc1)(C(=O)OCC)S(=O)(=O)c1ccc(OC)cc1
Reaction #184916
DOI: 10.1039/C8SC04228D
CCCCN1CCC(C(=O)OCC)(S(=O)(=O)c2ccc(OCCC(C)C)cc2)CC1
Reaction #188857
DOI: 10.1039/C8SC04228D
CCCCC1(CC)CN(c2ccccc2)c2cc(SCC(=O)OCC)c(OCC(=O)O)cc2S(=O)(=O)C1
Reaction #188867
DOI: 10.1039/C8SC04228D
CCOC(=O)CSc1ccc(Oc2ccc(Cl)cc2)cc1
Reaction #189235
DOI: 10.1039/C8SC04228D
COC(=O)CSc1ccc([N+](=O)[O-])c(N)c1
Reaction #194157
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)C2(C(=O)O)CCN(CCCc3ccccc3)CC2)cc1
Reaction #196008
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(Cc1ccc(OCCN2CCCCC2)cc1)S(=O)(=O)c1ccoc1C
Reaction #199989
DOI: 10.1039/C8SC04228D
COC(=O)c1nc2c(cc1F)SCC(=O)N2
Reaction #208529
DOI: 10.1039/C8SC04228D
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