子结构搜索

C=CCl

C=CCN(CC=C)C(=O)CCl
Reaction #3721
2-chloro-N,N-diallylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-c2ccc(C(F)(F)F)cc2)cc1C
Reaction #9734
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCC(Cl)=C1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC1.O=C(O)C(F)(F)F
Reaction #43783
72
收率 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CNCC=C1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC1.O=C(O)C(F)(F)F
Reaction #43784
221
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)C(Cl)=C(Cl)Cl)C(=O)c1ccccc1
Reaction #49915
N'-t-butyl-N-(1,2,2-trichlorovinyl)carbonyl-N'-benzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccc(-c2ccccc2)cc1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52288
title compound
收率 8.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ncc(Cl)cn1
Reaction #61051
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)Nc2cccc3c2C2CCC3C2=C(Cl)Cl)c(C(F)F)n1
Reaction #67691
pure product
收率 83.4%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)Nc2cccc3c2C2CCC3C2=C(Cl)Cl)c(C(F)F)n1
Reaction #67692
3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid (9-dichloromethylene-1,2,3,4-tetrahydro-1,4-methano-naphthalen-5-yl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74965
1,2,3,4,9,9-hexachloro-1,4-dihydro-5,8-dihydroxy-1,4-methanonaphth-6-yl methyl ketone
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(Cl)c(O)c2c1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74966
1,2,3,4,6,9,9-heptachloro-1,4-dihydro-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74968
crystals
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74974
1,2,3,4,11,11-hexachloro-1,4,4a,9a-tetrahydro-1,4-methanoanthracene-9,10-dione
DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cl)COc1ccc(Cl)cc1
Reaction #80586
1-(4-chlorophenoxy)-2-chloro-2-propene
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)Cc1ccccc1Oc1ccc(Cl)cc1
Reaction #80587
1-bromo-3-[(4-chlorophenoxy)phenyl]-2-propanone
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=CCl)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)C3=CC[C@@]21C
Reaction #94828
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1C2=CC[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CCl
Reaction #94829
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1CC)C(=O)C(Cl)=CC2=O
Reaction #177912
DOI: 10.1039/C8SC04228D
CC(C)C(CC=C(Cl)Cl)C(=O)O
Reaction #179959
DOI: 10.1039/C8SC04228D
CC1(C)C(=O)C(C(=O)c2ccc(C(F)F)c3ncccc23)=C(Cl)C(C)(C)C1=O
Reaction #182593
DOI: 10.1039/C8SC04228D
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