部分構造検索

Oc1ccc(Cl)cc1

FC(F)(F)C(F)(Cl)Oc1ccc(Cl)cc1
Reaction #4836
4-(1-chloro-1,2,2,2-tetrafluoroethoxy)chlorobenzene
収率 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc(Cl)cc2C1=S
Reaction #4906
product
収率 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)COc1cc(N)c(Cl)cc1C(=O)O
Reaction #5470
fine colorless needles
収率 68.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)cc2c1OC1CCCCC21
Reaction #5972
2-Chloro-5a,6,7,8,9,9a-Hexahydrodibenzofuran-4 -Carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc2c1O[C@@H]1CCCC[C@@H]21
Reaction #5985
METHYL 2-CHLORO-TRANS-5a,6,7,8,9,9a-HEXAHYDRODIBENZOFURAN-4-CARBOXYLATE
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)cc2c1O[C@@H]1CCCC[C@H]21
Reaction #5986
2-chloro-cis-5a,6,7,8,9,9a-hexahydrodibenzofuran-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CNCc1cc(F)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #6997
[2-(3,4-DICHLOROPHENOXY)-5-FLUOROBENZYL]-METHYLAMINE
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1CSC(C)=O
Reaction #11764
title compound
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1Cc2cc(Cl)c3ccccc3c2O1)OCc1ccccc1
Reaction #42219
(±)-benzyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42220
(±)-methyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamate
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42249
(±)-1-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methanamine
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42250
(±)-1-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)-N-methylmethanamine
収率 23.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(CCOc3ccc(Cl)cc3)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43832
{5-[[2-(4-Chloro-phenoxy)-ethyl]-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(Cl)cc1-c1ccc(C(=O)N2CCCC2)c(F)c1
Reaction #44372
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)NC(=O)c1ccc(-c2cc(Cl)ccc2O[C@@H](C)C(=O)O)cc1F
Reaction #44394
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)COc1ccccc1Oc1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+](=O)[O-]
Reaction #49801
title product
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=CC(=O)COc1ccccc1Oc1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+](=O)[O-]
Reaction #49802
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1Oc1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+](=O)[O-])OCc1ccccc1
Reaction #49803
title product
収率 77.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(Cl)c2c(=O)c3ccccc3sc12
Reaction #64673
title compound
収率 75.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(Cl)c2c(=O)c3ccccc3sc12
Reaction #64674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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