Substructure Search

C1CCCCC1

CCCN(CCC)C(=O)/C=C(\C)C(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCC2CCCCC2)CN1C(=O)O.Cl
Reaction #48756
title compound
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #51582
oligomer ( A1 )
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(=O)CC(C)(C)C1.CCC1=C(CC)C(=O)NC1=O.CCOC(N)=O.CCOC(N)=O
Reaction #52247
Isophorone Bisurethane Bisethylmaleimide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](OCCCBr)CC1
Reaction #53815
trans-[4-(3-Bromo-propoxy)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H]1CC[C@H](N(C)C(=O)OC(C)(C)C)CC1
Reaction #53854
trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #53855
12.83
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCC(=CCCCC(=O)O)CC1
Reaction #53938
5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acid
Yield 85.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #69116
solid
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)OC(C)(C)C)C1CCC(O)CC1
Reaction #69128
title compound
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)OC(C)(C)C)[C@H]1CC[C@@H](OS(C)(=O)=O)CC1
Reaction #69129
compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)C(=O)N[C@H]1CC[C@H]([C@@H](C)NC(=O)OC(C)(C)C)CC1
Reaction #69130
title compound
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)O.CCOC(N)=O
Reaction #72269
urethane acrylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc3nc(N[C@@H]4[C@H]5C[C@H]5C[C@@H]4NC(=O)OCC[Si](C)(C)C)ncc3c2)c1Cl
Reaction #84649
title compound
Yield 62.5%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)N[C@H]1C[C@@H]2C[C@@H]2[C@H]1N
Reaction #84688
title compound
Yield 80.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)O.CCOC(N)=O
Reaction #155364
Urethane Acrylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCC(COC(=O)N2CCCC2)CC1)c1ccccn1
Reaction #155666
compound
Yield 70.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #168364
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2c(Nc3ccccc3F)nc3cc(-c4noc(=O)[nH]4)nc(-c4cncc(Cl)c4)c32)CC1
Reaction #168369
3-(4-(5-chloropyridin-3-yl)-2-((2-fluorophenyl)amino)-3-((trans-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2cc(-c3ccc(O)cc3)nc3c2c(CCC2CCCCC2)nn3C2CCCCO2)CC1
Reaction #169233
title compound
Yield 95.4%DOI: 10.6084/m9.figshare.5104873.v1
COCCCCC(O)(c1cccc(C#N)c1)C1CCCN(C(=O)NC(CC2CCCCC2)CN(C)C(=O)OCC[Si](C)(C)C)C1
Reaction #176879
DOI: 10.1039/C8SC04228D
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