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CCCCCCCCCC(=O)Cl

CCCCCCCCCC(=O)Oc1ccc(C(=O)O)cc1
Reaction #848
p-decanoyloxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)Cl)[C@@]4(C)CC[C@@H]32)C1
Reaction #3185
3β-acetoxy-5-cholenic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)C(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #3186
3β-acetoxy-24-oxo-5-cholestene
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)N[C@@H](C)C(=O)N[C@H](CCC(=O)O)C(=O)OCc1ccccc1
Reaction #4517
stearoyl-L-Ala-D-Glu(OH)OBzl
Выход 196.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCCCCCCCCCCC(=O)Cl
Reaction #4580
isohexadecanoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)NC#N
Reaction #4588
6
Выход 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)NC#N
Reaction #4589
Stearoylcyanamide
Выход 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)NCCO
Reaction #5223
2-Palmitoylaminoethanol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5345
4-hydroxy-3-(1-oxooctadecyl)-2(5H)-furanone
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)CC(=O)OC
Reaction #5722
methyl-3-oxoeicosanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)NCCCSc1ccncc1
Reaction #6189
desired compound
Выход 72.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCC(=O)NCCCSc1ccncc1
Reaction #6190
desired compound
Выход 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)NCCCSc1ccncc1
Reaction #6191
desired compound
Выход 73.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)NCCCSc1ccncc1
Reaction #6192
desired compound
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(=O)NC(C)C(=O)O
Reaction #11352
2-Decanoylaminopropionic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)N[C@H](C(=O)O)C(C)C
Reaction #42002
N-lauroyl-L-valine
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)N[C@H](C(=O)O)C(C)C
Reaction #43894
N-lauroyl-L-valine
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)OC(CONC(=N)c1cccnc1)CN1CCCCC1.Cl
Reaction #48026
N-[2-palmitoyloxy-3-(1-piperidinyl)propoxy]-3-pyridinecarboximidamide monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCCOc1ccc(C2C(=O)Oc3c2cc(C(C)(C)C)cc3C(C)(C)C)cc1
Reaction #50778
5,7-di-tert-butyl-3-[4-(2-stearoyloxyethoxy)phenyl]benzofuran-2-one
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC12CCC(C(=O)Cl)(CC1)CC2
Reaction #51112
4-pentylbicyclo[2.2.2]octane-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
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