Substructure Search

CCOC(CC=C)OCC

CCOC(CCCc1cc(C(=O)NC2CC2)ccc1F)OCC
Reaction #6968
N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide
Yield 93.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=Cc1ccc(OC(F)=C(F)F)cc1)c1ccc(OC(F)=C(F)F)cc1
Reaction #50275
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOC1(OC(C)CCCCCC)C=CC(N=Nc2ccccc2)=CC1
Reaction #62534
4'-dodecyloxy-4'-(1-methyl-heptyloxy)-azobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)O)C1OC(C(C)C(O)C(C)C(=O)C(CC)C2OC3(C=CCC4(CCC(C)(C5CCC(O)(CC)C(C)O5)O4)O3)C(C)CC2C)C(C)CC1C
Reaction #74918
20-deoxynarasin
Yield 71.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1C=C(Br)C(=O)C(O)O1
Reaction #175399
DOI: 10.1039/C8SC04228D
CCOC(OCC)C(=O)C=Cc1cc(-c2nn(C)c(OC(F)F)c2Cl)ccc1Cl
Reaction #175986
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=Cc1ccccc1OC)C(=O)C(OCC)OCC
Reaction #232373
DOI: 10.1039/C8SC04228D
Cc1ccnc(N)c1C#N
Reaction #320771
2-amino-3-cyano-4-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1(OCc2cccc(Cl)c2)C=CC(NCC(N)=O)=CC1.Cl
Reaction #362102
[4-(3-chlorobenzyloxy)phenetyl]aminoacetamide, hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(Nc1ccccc1)(OCC)C1(Cl)C=CN=C(C(=O)c2ccccc2)C1
Reaction #367728
titled compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(Nc1ccccc1)(OCC)C1(F)C=CN=C(C(=O)c2ccc(Cl)cc2)C1
Reaction #367729
titled compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCCC(C)=CC=CC(C)C=O
Reaction #368755
DOI: 10.1039/C8SC04228D
CCOC(CC=C(C)C(=O)[O-])OCC
Reaction #451854
2,2 diethoxy-ethyl-methacrylate
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(C=O)NC(CF)=C(C(=O)OCC)C1c1cccc([N+](=O)[O-])c1
Reaction #452138
title compound
Yield 18.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1(CO)C=CC(CC(=O)Nc2ccccc2)=CC1
Reaction #547305
yellow oil
Yield 149.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@H](OCC)O[C@@H]1CO
Reaction #552884
(2S-cis)-tetrahydro-5-ethoxy-3-methylene-2-furanmethanol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C(=O)OC)C=CC(C2OCCCCO2)=CN1
Reaction #570797
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)C(=O)C=Cc1cc(-c2nn(C)c(OC(F)F)c2Cl)ccc1Cl
Reaction #670220
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=Cc1ccccc1Cl)C(=O)C(OCC)OCC
Reaction #701762
ethyl 2-(2-chlorobenzylidene)-4,4-diethoxyacetoacetate
Yield 106.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=Cc1ccccc1Cl)C(=O)C(OCC)OCC
Reaction #701763
ethyl 2-(2-chlorobenzylidene)-4,4-diethoxyacetoacetate
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next