Substructure Search

CCCCOC(=O)CCC

CCCCCCCCCCOc1cnc(-c2ccc(CCCC(OC(=O)CCCCCCCC)C(F)(F)F)cc2)nc1
Reaction #1260
4-(4-nonanoyloxy-5,5,5-trifluoro-1-pentyl) phenyl-5-decyloxypyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)O[C@H]1CC[C@H](c2ccc(CN(C)C)cc2)CC1
Reaction #1749
trans-O-butyryl-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)O
Reaction #5384
Oleic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OCC(CO)CCn1cnc2cnc(N)nc21
Reaction #5966
2-amino-9-(4-butyryloxy-3-hydroxymethylbut-1-yl)purine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)oc2c(C=CCCl)c(O)ccc12
Reaction #53759
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)CC(C)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55181
3-(2',4'-difluoro-4-biphenylyl)butyric acid n-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C1OC(OCC)C=CC1C
Reaction #56362
butyl-3-methyl-6-ethoxy-3,6-dihydro-2H-pyran-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)CCC
Reaction #56512
butylbutyrate
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)C(=O)O[C@H]1C[C@H](O)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@H]21
Reaction #59804
Pravastatin
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CCC)C(=O)OCCCCO
Reaction #70095
oil
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=Cc1ccccc1)C(=O)O
Reaction #75273
α-ethyl cinnamic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)OCc1ccccc1)O[C@@H]1O[C@@H](C)[C@H](OC(=O)[C@H](C)CN=[N+]=[N-])C[C@H]1OC(=O)CCCCO[C@@H]1O[C@@H](C)[C@H](OCc2ccccc2)C[C@H]1OCc1ccccc1
Reaction #90247
(2R,3R,5R,6S)-5-(((R)-3-azido-2-methylpropanoyl)oxy)-2-(((R)-5-(benzyloxy)-5-oxopentan-2-yl)oxy)-6-methyltetrahydro-2H-pyran-3-yl 5-(((2R,3R,5R,6S)-3,5-bis(benzyloxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)pentanoate
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC=CCCCCCCCCN1CCN=CCCC1=O
Reaction #95958
4-(9-octadecenyl)-2,3,6,7-tetrahydro-1,4-diazocin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)CCC(=O)N[C@@H](CC(=O)OCc1ccccc1)Cc1ccc(-c2cccc(Cl)c2)cc1
Reaction #158010
(R)-benzyl 3-(4-butoxy-4-oxobutanamido)-4-(3′-chlorobiphenyl-4-yl)butanoate
Yield 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(N)=O.N[C@@H](Cc1ccccc1)C(=O)O
Reaction #159282
phenylalanine butyramide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)[C@H](Cc1ccccc1)Nc1ccccc1
Reaction #164155
titled product
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[N+]12CCC(CC1)[C@@H](OC(=O)[C@@H](Cc1ccccc1)Nc1ccccc1)C2)c1ccccc1.[Br-]
Reaction #164214
title compound
Yield 98.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)OC(CCc2ccc(OCc3ccccc3)cc2)(C2CCCC2)C1
Reaction #174574
DOI: 10.1039/C8SC04228D
[I-]
Reaction #174937
DOI: 10.1039/C8SC04228D
O=C1CCCCCCC(=O)O1
Reaction #179543
DOI: 10.1039/C8SC04228D
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