Substructure Search

CCCCCCCCCCO

C=C(C)C(=O)OCCCCCCCCCCCC.C=CN1CCCC1=O
Reaction #1498
lauryl methacrylate N-vinyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCC(=O)OC(C)C
Reaction #1500
isopropyl myristate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[C@@H](F)COc1c(F)cc([C@H]2CC[Si@H]([C@H]3CC[C@H](CCC(C)C)CC3)CC2)cc1F
Reaction #2739
(R)-4-(trans-4-(trans-4-(3-methylbutyl)cyclohexyl)-4-silacyclohexyl)-1-(2-fluorodecyloxy)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[C@@H](F)COc1c(F)cc(-c2ccc([C@H]3CC[Si@H](CCCCC)CC3)cc2)cc1F
Reaction #2741
(R)-4-(4-(trans-4-n-pentyl-4-silacyclohexyl)phenyl)-1-(2-fluorodecyloxy)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC
Reaction #4991
Dodecyl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1C[C@H]1CC(=O)O
Reaction #5365
cis-2-(2'-pentylcyclopropyl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1C[C@H]1CC(=O)O
Reaction #5366
cis-2-(2'-pentylcyclopropyl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cl)(Cl)C12CC3CC(CC(C3)C1)C2
Reaction #57416
adamantan-1-yl-dichloro-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cl)(Cl)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57417
dichloro-(3-hydroxy-adamantan-1-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57418
a-oxotricyclo[3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(O)C1
Reaction #62539
menthol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOP(=O)(O)O[C@H](CC(=O)O)C[N+](C)(C)C.[OH-]
Reaction #64412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64421
salt
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC
Reaction #71258
Cetyl Stearate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)O.OCCN(CCO)CCO
Reaction #71259
Triethanolamine Stearate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCC1CC1
Reaction #72408
7-cyclopropylheptanoic acid
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(=O)NN
Reaction #78019
decanoic acid hydrazide
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(Oc3c(F)c(F)c(C(F)(F)F)c(F)c3F)=CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81460
title compound
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81461
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCCCCC(C)Oc1cccc(I)c1
Reaction #81778
ethyl 10-(3-iodophenoxy)-undecanoate
Yield 33.3%DOI: 10.6084/m9.figshare.5104873.v1
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