Substructure Search

16719

CCCCCC(N)CC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
Reaction #2072
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(N)CC(P(=O)([O-])[O-])P(=O)([O-])O.[NH4+].[NH4+].[NH4+]
Reaction #2073
3-aminooctane-1,1-bisphosphonic acid, triammonium salt
Yield 419.8%DOI: 10.6084/m9.figshare.5104873.v1
NCC(CP(O)O)C1CCCCC1
Reaction #5276
3-amino-2-cyclohexylpropylphosphonous acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)P(=O)(CC(CN)C1CCCCC1)OCC
Reaction #5279
ethyl 3-amino-2-cyclohexylpropyl(diethoxymethyl)phosphinate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCP(=O)(O)CCCCCCCC
Reaction #9611
di-n-octylphosphinic acid
Yield 48.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[PH](=O)O
Reaction #9612
n-octylphosphinic acid
Yield 84.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C1CC[C@H]2CCC[C@@H](c3ccc(Cl)cc3)N2C1=O
Reaction #44646
[(6S,9aR)-6-(4-chlorophenyl)-4-oxooctahydroquinolizin-3-yl]phosphonic acid diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C2\CC[C@H]3CCC[C@@H](c4ccc(Cl)cc4)N3C2=O)ccc1-n1cnc(C)c1
Reaction #44647
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCP(=O)([O-])[O-].[Ba+2]
Reaction #56113
white powder
Yield 96.3%DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(CC(=O)CCC1CCCC1)OC
Reaction #57063
product
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(CC(=O)[C@@H](C)CCCCc1ccccc1)OC
Reaction #87984
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(CC(=O)[C@@H](C)CCCCCc1ccccc1)OC
Reaction #87985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)CP(=O)(OC)OC
Reaction #94520
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCCCCCCCCCN1C(=O)c2ccccc2C1=O)OCC
Reaction #172173
diethyl 12-(1,3-dioxoisoindolin-2-yl)dodecylphosphonate
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCCCCCCCCCCP(=O)(O)O
Reaction #172174
solid
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCP(=O)([O-])[O-].[K+].[K+]
Reaction #172183
Potassium octadecylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCCCCCCCCOCc1ccccc1)OCC
Reaction #172184
desired product
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=P(O)(O)CCCCCCCCCCCOCc1ccccc1
Reaction #172185
11-(benzyloxy)undecylphosphonic acid
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=P(O)(O)CCCCCCCCCCOCCCCCCCCOCc1ccccc1
Reaction #172186
solid
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=P(O)(O)CCCCCCCCCCCOC(F)(F)c1c(F)c(F)c(F)c(F)c1F
Reaction #172187
11-(perfluorobenzyloxy)undecylphosphonic acid
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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