Teilstruktursuche

CNN=Cc1ccccc1

c1ccc(C2=NNCC2)cc1
Reaction #40769
yellow oil
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
Cc1ccc(-c2nc(-c3ccccc3Cl)nn2C)cc1Oc1ccc(C(F)(F)F)cn1
Reaction #80514
desired compound
Ausbeute 36.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(Cl)c1/C=N/Nc1ccc(I)cc1
Reaction #87505
desired product
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(Cl)c1C(Cl)=NNc1ccc(I)cc1
Reaction #87506
desired product
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1S(=O)(=O)OCC(=NNc1ccccc1)c1ccccc1
Reaction #94132
3,5-dimethoxy-4-benzenesulphonyloxy-acetophenone phenylhydrazone
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC/C(=N/Nc1ccccc1)c1ccc(Br)cc1F
Reaction #155873
(Z)-1-(1-(4-bromo-2-fluorophenyl)propylidene)-2-phenylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(-c2ccccc2)c2cc(Br)ccc12
Reaction #155874
6-bromo-3-ethyl-1-phenyl-1H-indazole
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=N/Nc1ccccc1)c1ccc(Br)cc1F
Reaction #155884
(Z)-1-(1-(4-bromo-2-fluorophenyl)ethylidene)-2-phenylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccccc2)c2cc(Br)ccc12
Reaction #155885
6-bromo-3-methyl-1-phenyl-1H-indazole
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1NN=C(c2cccc(Nc3nc(Cl)ncc3F)c2)O1
Reaction #158478
2-chloro-N4-[3-(2-ethoxycarbonylmethylene-1,3,4-oxadiazol-5-yl)phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1NN=C(c2cccc(Nc3nc(Cl)ncc3F)c2)O1
Reaction #163588
2-chloro-N4-[3-(2-ethoxycarbonylmethylene-1,3,4-oxadiazol-5-yl)phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)C(=O)N(C2CCN(C(=O)c3cc(OCc4ccccc4)ccc3C)CC2)N=C1c1ccc(OC)c(OC)c1
Reaction #174306
DOI: 10.1039/C8SC04228D
COc1ccc(C2=NN(C3CCN(S(=O)(=O)c4ccc5c(ccn5C)c4)CC3)C(=O)C2(C)C)cc1OC
Reaction #175514
DOI: 10.1039/C8SC04228D
CCOc1cc(C2=NN(C(=O)c3sc(-c4ccccn4)nc3C)CCC2)ccc1OC
Reaction #176686
DOI: 10.1039/C8SC04228D
c1ccc(C2=NNCC2)cc1
Reaction #178437
DOI: 10.1039/C8SC04228D
COc1ccc(C2=NN(C3CCN(C(=O)c4ccccc4Cl)CC3)C(=O)C2(C)C)cc1OC
Reaction #179309
DOI: 10.1039/C8SC04228D
[C-]#[N+]C1(C)CN(C(=O)Nc2ccc(C(F)(F)F)cc2)N=C1c1ccc(Cl)cc1
Reaction #180431
DOI: 10.1039/C8SC04228D
COC(=O)N(C)N=C(c1ccc(Cl)cc1)C(C)(C)C
Reaction #180813
DOI: 10.1039/C8SC04228D
COc1cccc(C(=O)N2CCC(N3N=C(c4ccc(OC)c(OC)c4)C(C)(C)C3=O)CC2)c1
Reaction #181206
DOI: 10.1039/C8SC04228D
Seite 1Weiter