hydrogen peroxide water

O=C([O-])C1OC1C(=O)[O-].[K+].[K+]
Reaction #8648
potassium epoxysuccinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(O)cnc1F
Reaction #168830
6-fluoro-5-methylpyridin-3-ol
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCN1C(=O)C2CC3OC3CC2C1=O
Reaction #338694
4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide
收率 1000.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(OCCCCC(F)(F)C(F)(F)S(=O)(=O)[O-])C1CCCCC1.[Na+]
Reaction #420293
sodium 1,1,2,2-tetrafluoro-6-cyclohexylcarbonyloxyhexane-1-sulfonate
收率 224.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)ON=C(C(N)=O)C(=NOC(C)C)n1cncn1
Reaction #426611
title compound
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCCCCCCCCCCS(=O)(=O)c1cc(Cl)ccc1[N+](=O)[O-]
Reaction #516686
2-n-dodecylsulfonyl-4-chloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCCc1c(Cc2ccc(-c3ccccc3C#N)cc2F)c(=O)n([C@H]2CC[C@H](OCC3(O)CCC3)CC2)c2ncnn12
Reaction #606818
title compound
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCCc1c(Cc2ccc(-c3ccccc3C#N)cc2)c(=O)n([C@H]2C[C@H](O)C2)c2ncnn12
Reaction #606825
title compound
收率 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCCc1c(Cc2ccc(-c3ccccc3C#N)cc2)c(=O)n([C@H]2C[C@@H](O)C2)c2ncnn12
Reaction #606826
title compound
收率 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(NC(=O)OCc1ccccc1)c1ccc(-c2ccc([C@@H](OP(=O)(OCc3ccccc3)OCc3ccccc3)[C@@H](CF)NC(=O)C(F)F)cc2)cn1
Reaction #612798
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1cc(C)c(C)[n+]([O-])c1
Reaction #665229
title compound
收率 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCOc1ccc2c(c1F)C(F)(F)C(F)(F)c1c-2ccc(O)c1F
Reaction #805687
7-ethoxy-1,8,9,9,10,10-hexafluoro-9,10-dihydrophenanthrene-2-ol
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Oc1cnc(F)c(F)c1
Reaction #960243
title product
收率 29.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)N1Cc1ccccc1S(C)(=O)=O
Reaction #976035
title compound
收率 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COc1c(Cl)cc[n+]([O-])c1C
Reaction #1148621
4-chloro-3-methoxy-2-methylpyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_02
CNC(=O)c1cc(COc2nnc(Nc3ccc(Cl)cc3)c3ccccc23)ccn1
Reaction #1157711
desired compound
收率 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_06
C=CCN1C(=O)C2CC3OC3CC2C1=O
Reaction #1183649
4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide
收率 7289.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1C(=O)N[C@@H]1[C@@H](C)C(=O)O
Reaction #1338181
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_01
CCN(CC)c1ccc(N=Nc2ncc(C(F)(F)F)cc2Cl)c(O)c1
Reaction #1354117
2-(3-chloro-5-trifluoromethyl-2-pyridylazo)-5-(diethylamino)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CCN(CC)c1ccc(N=Nc2ncc(Cl)cc2Cl)c(O)c1
Reaction #1354119
2-(3,5-dichloro-2-pyridylazo)-5-(diethylamino)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
第 1 页下一页