diethyl (hydroxymethyl)phosphonate

CCOP(=O)(COC(=O)c1ccc(Cl)cc1OC)OCC
Reaction #202502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOP(=O)(COc1ccc(Br)cc1[N+](=O)[O-])OCC
Reaction #211000
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOP(=O)(COCc1sc(Cl)nc1Cl)OCC
Reaction #264102
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(COc1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-])OCC
Reaction #268997
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(CO[Si](C)(C)C(C)(C)C)OCC
Reaction #269403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCc1nc(Cl)c(C(=O)OCP(=O)(OCC)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #309723
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCOP(=O)(COS(=O)(=O)c1c(C)cccc1Cl)OCC
Reaction #384617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOP(=O)(COCc1nc2c(N)ncnc2n1CCc1ccccc1)OCC
Reaction #387056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOP(=O)(COS(=O)(=O)c1c(C)cccc1Cl)OCC
Reaction #414184
oil
المردود 87.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCOP(=O)(COS(=O)(=O)c1ccccc1C(F)(F)F)OCC
Reaction #414185
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
C=CCOCP(=O)(OCC)OCC
Reaction #432242
diethyl allyloxymethylphosphonate
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
CCOP(=O)(COCc1csc(C)n1)OCC
Reaction #441204
2-methyl-4-(diethylphosphonomethoxymethyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CCOP(=O)(Cc1cc(C)cc(C)n1)OCC
Reaction #441208
2-diethylphosphonomethyl-4,6-dimethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CCOP(=O)(COc1ccc(Br)cc1[N+](=O)[O-])OCC
Reaction #441231
2-diethylphosphonomethyloxy-5-bromonitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CCOP(=O)(COC(=O)[C@@H](C)c1ccc2cc(OC)ccc2c1)OCC
Reaction #466281
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCCCc1nc(Cl)c(C(=O)OCP(=O)(OCC)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #471764
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C(CCl)COCP(=O)(OCC)OCC
Reaction #485951
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCOP(=O)(COC/C=C\CCl)OCC
Reaction #485953
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCOP(=O)(COCC#CCCl)OCC
Reaction #485955
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCOP(=O)(CO[Si](C)(C)C(C)(C)C)OCC
Reaction #575348
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
الصفحة 1التالي