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CCCCCCCBr

BrCCCCCCC1CCCCC1
Reaction #9908
(6-bromo-hexyl)-cyclohexane
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN1CCC[C@H]1c1ccc[n+](CCCCCCC2CCCCC2)c1.[Br-]
Reaction #9909
(S)-1-(6-cyclohexyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
Выход 63.3%DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCCCCCCCn1c2ccccc2c2ccccc21
Reaction #11838
N-(10-bromodecyl)-carbazole
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)C(CCCCCCCCCCn1c3ccccc3c3ccccc31)(CCCCCCCCCCn1c3ccccc3c3ccccc31)c1cc(Br)ccc1-2
Reaction #11840
title product
Выход 34.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCCOc1ccc(C(=O)OC)cc1
Reaction #49716
Methyl 4-docosyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCBr)cccc21
Reaction #50069
6-bromohexylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCN3CCOCC3)cccc21
Reaction #50070
6-morpholinylhexylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCCBr)cccc21
Reaction #50072
7-bromoheptylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCCN3CCOCC3)cccc21
Reaction #50073
7-morpholinylheptylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCCCBr)cccc21
Reaction #50075
8-bromooctylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCCCN3CCOCC3)cccc21
Reaction #50076
8-morpholinyloctylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCNCC1CCCCCCc1cccc2c1C(=O)NC2=O
Reaction #50086
6-(N-methylpiperazinyl)hexylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCNCC1CCCCCCCCc1cccc2c1C(=O)NC2=O
Reaction #50088
8-(N-methylpiperazinyl)octylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c(CCCCCCCCN3CCCC3)cccc21
Reaction #50090
8-pyrrolidinyloctylphthalimide
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CCCCCCCCBr)cc1
Reaction #50713
8-(4-hydroxyphenyl)octylbromide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)OB(O)c1ccc(CCCCCCCCCCCO)cc1
Reaction #53274
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53928
trans-4-(5-Bromo-pentyl)-cyclohexylamine
Выход 129.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(N[C@H]1CC[C@H](CCCCCBr)CC1)c1ccc(C(F)(F)F)cc1
Reaction #53929
trans-N-[4-(5-Bromo-pentyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53935
trans-[4-(5-Bromo-pentyl)-cyclohexyl]-methyl-amine hydrobromide
Выход 179.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1CC[C@H](CCCOc2ccc(C=O)cc2)CC1
Reaction #64066
4-[3-(trans-4-pentylcyclohexyl)-1-propyloxy]benzaldehyde
Выход 121.9%DOI: 10.6084/m9.figshare.5104873.v1
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