Substructure Search

326066

CCCCCCCCNC(=O)Nc1nc2nc(NCCCN3CCN(C)CC3)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3530
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCNC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10121
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}(octylamino)carboxamide
Yield 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCNC(=O)NOCC(O)CN1CCCCC1
Reaction #48027
N-[2-hydroxy-3-(1-piperidinyl)propoxy]-N′-heptyl-urea
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
CCOC(N)=O.NC(N)=O
Reaction #54176
urethane urea
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65588
4-Hydroxy-2-oxo-2.5-dihydro-furan-3-carboxylic acid-2-cyclododecyl-ethylamide
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
CCn1c2c(c3ccccc31)CCCC2(CC)CCN
Reaction #93906
title compound
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=NC1C2CC3CC(C2)CC1C3
Reaction #159302
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCN(C(=O)NC2C3CC4CC(C3)CC2C4)C1
Reaction #159316
(R)-tert-butyl 1-(2-adamantylcarbamoyl)pyrrolidin-3-ylcarbamate
Yield 19.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172734
title compound
Yield 86.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCC3(NC(=O)OC(C)(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172735
title compound
Yield 66.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)NCCN(C)C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172736
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)NC3(C(=O)O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172738
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)NCC(C)(C)N3CCOCC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172739
title compound
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)N3CCN([C@@H]4COC[C@H]4N(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172740
title compound
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)c(F)c6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12.Cl.Cl
Reaction #172874
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172944
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-isocyanato-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol
Yield 78.1%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next