Substructure Search

CCCCCCI

CCCCCCOc1cc2ccc(-c3ccc(C(=O)OC)c(O)c3)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1230
methyl 2-hydroxy-4-[7-(1-adamantyl)-6-hexyloxy-2-naphthyl]benzoate
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCCCCCCCCCCOc1ccc(C(=O)O)cc1
Reaction #5259
4-(10-allyloxydecyloxy)benzoic acid
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCCCCCI)C(=O)OC(C)(C)C
Reaction #5510
t-butyl methyl 7-iodoheptylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCI)CCc4cc(F)ccc43)c[nH]c12
Reaction #41996
title compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCC1(c2c[nH]c3c(NS(C)(=O)=O)cccc23)CCc2cc(F)ccc21
Reaction #41997
title compound
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCN4CCOCC4)CCc4cc(F)ccc43)c[nH]c12
Reaction #41998
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CI)CCCC1
Reaction #44866
title compound
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CN2CCC(CNC(=O)OC(C)(C)C)CC2)CCCC1
Reaction #44867
title compound
Yield 67.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CN2CCC(O)(CNC(=O)OC(C)(C)C)CC2)CCCCC1
Reaction #44875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCCCCCI)C(=O)OC(C)(C)C
Reaction #50265
t-butyl methyl 7-iodoheptylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCN(C(=O)C(C)C)c1sc(CC)cc1C(=O)OCC
Reaction #55940
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OCCCCCCOc1ccc(CO)cc1
Reaction #56593
4-(6-acryloyloxyhexyloxy)benzylalcohol
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OCCCCCCOc1ccc(N=Nc2ccc(N=Nc3ccc(N(C)C)c4ccccc34)cc2)c2ccccc12
Reaction #56595
1-[4-(4-(dimethylamino)naphthylazo)-phenylazo]-4-(6-acryloyloxyhexyloxy)naphtalene
Yield 84.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOc1ccc2[nH]c(C)c(CC(=O)O)c2c1
Reaction #65985
white crystals
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)OCCOCC=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #66011
2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundec-2-enyloxy)ethyl hydrogen sulfate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CC(=O)[C@@H]1Cc1cccc(OCc2ccccc2)c1)O[Si](C)(C)C(C)(C)C
Reaction #67887
(2R,3R,4R)-2-(3-(benzyloxy)benzyl)-4-tert-butyldimethylsilyoxy-3-((S)-3-tert-butyldimethylsilyoxyoctyl)cyclopentanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Yield 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Yield 64.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81467
17-(3-Pyridyl)androsta-5,16-dien-3β-ol
DOI: 10.6084/m9.figshare.5104873.v1
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