Recherche de Sous-structure

CO.ClCCl

N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2848
title compound
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)cc(NC(=O)C=NO)c1
Reaction #3203
title compound
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(O)cc(C=C(Cl)Cl)n1
Reaction #4002
2-amino-4-(2,2-dichloro-vinyl)-6-hydroxypyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)cc(C=C(Cl)Cl)n1
Reaction #4004
2-amino-4-chloro-6-(2,2-dichlorovinyl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4535
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4536
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Rendement 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4537
colorless crystals
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4540
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)C(F)(Cl)Oc1ccc(Cl)cc1
Reaction #4836
4-(1-chloro-1,2,2,2-tetrafluoroethoxy)chlorobenzene
Rendement 89.8%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCc2ccccc21
Reaction #5523
1-carbamylindoline
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC1(O)CCc2ccccc2C12CCCC2)OCC(Cl)(Cl)Cl
Reaction #5638
title compound
Rendement 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(ccc(F)c2F)N1C(=O)C=NO
Reaction #10434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(Cl)(Cl)Cl)N1CCc2ccccc2C1
Reaction #51099
title compound ( D6 )
Rendement 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)C=NO)cc1
Reaction #52596
N-(2-hydroximino-acetyl)anisidine
Rendement 85.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)C=NO)cc1
Reaction #52642
N—(2-hydroximinoacetyl)anisidine
Rendement 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1ccc(OC)cc1)Oc1ccc(OC)cc1
Reaction #56391
Ethyl 2,2-bis(4-methoxyphenoxy)-acetate
Rendement 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1ccc(C)cc1)Oc1ccc(C)cc1
Reaction #56392
Ethyl 2,2-bis(4-methylphenoxy)acetate
Rendement 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Sc1ccc(C)cc1)Sc1ccc(C)cc1
Reaction #56393
Ethyl 2,2-bis(4-methylthiophenoxy)acetate
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=NO)Nc1ccc2c(c1)CCC2
Reaction #59636
expected product
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOP(=O)(O)O[C@H](CC(=O)O)C[N+](C)(C)C.[OH-]
Reaction #64412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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