Substructure Search

770115

CCc1ccccccc(C(C)CC)[sH+]1.[Cl-]
Reaction #44411
title compound
Yield 6.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC=CCCCCCC
Reaction #45003
7-tetradecene
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)C1(c3ccccc3-c3ccccc31)c1ccccc1-2
Reaction #53766
white solid
Yield 97.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63581
intermediate 10
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)CC1(C(F)(F)F)Oc2ccc(Br)cc2O1
Reaction #65847
5-Bromo-2-(2,2,2-trifluoroethyl)-2-trifluoromethyl-1,3-benzodioxole
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1ccc([N+](=O)[O-])cc1
Reaction #66476
(RS)-1-(methylsulfinyl)-4-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C23CC4CC(CC(C4)C2)C3)cc1-c1cc(C23CC4CC(CC(C4)C2)C3)ccc1C
Reaction #69566
2,2′-dimethyl-5,5′-bis(1-adamantyl)biphenyl
Yield 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC=CCCCCCC
Reaction #71507
7-tetradecene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CN2CCOc3cc(N)ccc32)c1
Reaction #71865
crude title compound
Yield 87.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2CCOc3cc(N)ccc32)cc1
Reaction #71869
crude title compound
Yield 87.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1CCN(C)CC1)NC(C)=O
Reaction #75543
methyl 2-(acetylamino)-3-(4-methyl-piperazinyl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc([N+](=O)[O-])cc1Cl
Reaction #80484
desired compound
Yield 118.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOc1cc(-c2nc(-c3c(F)cccc3Cl)nn2C)ccc1Cl
Reaction #80493
desired compound
Yield 41.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1cc(-c2nc(-c3ccccc3Cl)nn2C)ccc1Cl
Reaction #80494
desired compound
Yield 42.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(-c2ccc(OC(F)(F)F)cc2)cc1Cl
Reaction #80495
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Cc2ccc(Cl)c(Cl)c2)c(Cl)c1
Reaction #80496
desired compound
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Oc2ccccc2)cc1Cl
Reaction #80500
desired compound
Yield 4.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2F)nc1-c1ccc(Cl)c(Oc2ccc(C(F)(F)F)cn2)c1
Reaction #80507
desired compound
Yield 24.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Cl)c(Oc2ccc(C(F)(F)F)cn2)c1
Reaction #80508
desired compound
Yield 31.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2ccccc2Cl)nc1-c1ccc(Oc2ccc(C(F)(F)F)cn2)cc1Cl
Reaction #80509
desired compound
Yield 67.3%DOI: 10.6084/m9.figshare.5104873.v1
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