Methyldichlorophosphate

COc1nc(C=CC#N)ccc1-n1cnc(C)c1
Reaction #277492
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1ccc2c(c1)OP(=O)(OC)O2
Reaction #323395
5-ethoxycarbonyl-2-methoxy-2-oxo-1,3,2-benzo-dioxaphosphole
Выход 84.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COP1(=O)Oc2ccc(C)cc2O1
Reaction #323396
2-methoxy-5-methyl-2-oxo-1,3,2-benzodioxaphosphole
Выход 88319.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COP1(=O)Oc2ccccc2O1
Reaction #323397
methyl o-phenylene phosphate
Выход 129.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COP1(=O)Oc2ccccc2O1
Reaction #386875
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#CC(CCCCl)c1ccc(Cl)cc1C(F)(F)F
Reaction #493549
title compound
Выход 79.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)(C)[Si](OCCC(CC#N)c1ccc(C(F)(F)F)cc1)(c1ccccc1)c1ccccc1
Reaction #493555
title compound
Выход 97.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #504948
N-methylpyridinium dichlorophosphate
Выход 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #531812
N-methylpyridinium dichlorophosphate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1nc(/C=C/C#N)ccc1-n1cnc(C)c1
Reaction #633942
title compound
Выход 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
COc1cc2c(c(OC)c1OC)-c1ccc(OP(=O)(O)OC)cc1[C@@H](NC(C)=O)CC2
Reaction #808138
(5S)-5-(acetylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-3-yl methyl hydrogen phosphate
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
C[n+]1ccccc1
Reaction #906957
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #975871
N-methylpyridinium dichlorophosphate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #1003705
N-methylpyridinium dichlorophosphate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
CCOC(=O)c1ccc2c(c1)OP(=O)(OC)O2
Reaction #1231274
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #1244257
N-methylpyridinium dichlorophophate
Выход 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #1279637
N-methylpyridinium dichlorophosphate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
C[n+]1ccccc1.O=P([O-])(Cl)Cl
Reaction #1461688
N-methylpyridinium dichlorophophate
Выход 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
O=P([O-])(Cl)Cl
Reaction #1647844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=C1C2CC3CC(C2)CC1C3)c1cccc(OP(=O)([O-])OCc2cc(OC)c(OC)cc2[N+](=O)[O-])c1.c1cc[nH+]cc1
Reaction #1689228
pyridinium 4,5-dimethoxy-2-nitrobenzyl 3-(methoxytricyclo[3.3.1.13,7 ]dec-2-ylidenemethyl)phenyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
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