Substructure Search

COC(=O)CCCCCOc1ccc(N)cc1

CCOC(=O)CCCCCOc1ccc(Nc2ccncc2)cc1
Reaction #2332
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCOc1ccc(N(C(=O)OC(C)(C)C)c2ccncc2)cc1
Reaction #2334
ethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(C)=O)cc1
Reaction #170968
15
Yield 42206.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ccc(OCCCCCC(=O)O)cc1
Reaction #170969
16
Yield 55.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(N)cc1
Reaction #170970
17
Yield 43.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(N)cc1
Reaction #170971
17
Yield 78.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(N=C=O)cc1
Reaction #170972
18
Yield 72.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(=O)OCCO)cc1
Reaction #170973
19
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(=O)OCCOC(=O)Nc2ccc(OCCCCCC(=O)OC)cc2)cc1
Reaction #170974
20
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
Reaction #170975
21
Yield 65.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCOc1ccc([N+](=O)[O-])cc1
Reaction #170986
35
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCOc1ccc([N+](=O)[O-])cc1)OCCO
Reaction #170987
6-(4-Nitrophenoxy)-hexanoic acid 2-hydroxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #170999
53
Yield 22.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(=O)CO)cc1
Reaction #171000
54
Yield 65.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(=O)CCCCCO)cc1
Reaction #171003
62
Yield 62.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCOc1ccc(NC(=O)OCCO)cc1
Reaction #174920
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCOc1ccc([N+](=O)[O-])c(Nc2ccc(C)cc2)c1
Reaction #189977
DOI: 10.1039/C8SC04228D
O=C(CCCCCOc1ccc([N+](=O)[O-])cc1)OCCO
Reaction #231507
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC1C(Oc2ccc([N+](=O)[O-])cc2C2OCCO2)OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C
Reaction #259804
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCOc1ccc(Nc2ccncc2)cc1
Reaction #353937
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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