子结构搜索

CNO

Cc1cc(Nc2cc(Nc3ccccc3C(=O)NOCCO)c(C(F)(F)F)cn2)n(C)n1
Reaction #307
收率 48.6%
CSc1cccc(NC(=O)c2cccc([N+](=O)[O-])c2)c1
Reaction #2538
title compound
收率 94.6%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOC(=NOC)c1ccc(Cl)cc1Cl
Reaction #3501
propargyl N-methoxy-2,4-dichlorobenzimidate
收率 29.8%DOI: 10.6084/m9.figshare.5104873.v1
[C-]#[N+]Cc1noc(C2CC2)n1
Reaction #4804
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1nc2ccc([N+](=O)[O-])cc2cc1C
Reaction #6901
N-ethyl-3-methyl-6-nitroquinolin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1nc2ccc(N)cc2cc1C
Reaction #6902
N2-ethyl-3-methylquinoline-2.6-diamine
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)c1ccccc1F
Reaction #41696
compound
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)c1ccc(N)cc1F
Reaction #41697
4-amino-2-fluoro-N-methoxy-N-methylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cc([N+](=O)[O-])ccc2s1
Reaction #43745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cccc([N+](=O)[O-])c2s1
Reaction #43763
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC=C(CNCCO)O1
Reaction #50507
2-(2-methyl-5-isoxazolylmethylamino)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)Cn1cc(S(N)(=O)=O)c2cc([N+](=O)[O-])ccc21
Reaction #51685
2-(5-nitro-3-sulfamoyl-indol-1-yl)-acetamide
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(O)CCNC(=O)c1cccc(Cl)c1Cl
Reaction #52093
title compound
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(O)CCNC(=O)c1cc(Cl)ccc1Cl
Reaction #52099
title compound
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(O)CCNC(=O)c1cc(Br)ccc1Cl
Reaction #52102
title compound
收率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1n[nH]c2ccc(N)cc12
Reaction #53669
5-amino-3-methylsulfonylamino-1H-indazole
收率 44.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1n[nH]c2ccc([N+](=O)[O-])cc12
Reaction #53670
3-methylsulfonylamino-5-nitro-1H-indazole
收率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2ccc(F)cc2)c(C(=O)O)c1
Reaction #58286
2-(4-fluorobenzoyl)-5-methoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc3c(c2)SCC(c2ccccc2)O3)nc1
Reaction #59594
5-Nitro-2-(2-phenyl-2,3-dihydrobenzo[1,4]oxathiin-6-yloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc3c(c2)S(=O)CC(c2ccccc2)O3)nc1
Reaction #59595
5-Nitro-2-(4-oxo-2-phenyl-3,4-dihydrobenzo[1.4]oxathiin-6-yloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
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