sodium dihydrogen phosphate

O=C(O)c1cc(-c2ccc(C(F)(F)F)cc2)cs1
Reaction #9736
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn([C@@H]3O[C@H](C(=O)O)[C@H]4OC(C)(C)O[C@H]43)c2n1
Reaction #10565
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #51103
2s
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(O)c1c(C2CC2)cc(C(F)(F)F)cc1C(F)(F)F
Reaction #67708
2-Cyclopropyl-4,6-bis-trifluoromethyl-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(=O)n(CC2OCCO2)c2cc(OC)ccc12
Reaction #67950
methyl 1-(1,3-dioxolan-2-ylmethyl)-7-methoxy-2-oxo-1,2-dihydroquinoline-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1c(I)ccn(-c2ccc(F)cc2)c1=O
Reaction #70999
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1[nH]c(C(=O)O)nc1C(F)(F)F
Reaction #71747
title compound
Ausbeute 118.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1[nH]c(C(=O)O)nc1C(F)(F)F
Reaction #71753
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1nc(C(=O)O)[nH]c1CC
Reaction #71767
title compound
Ausbeute 9.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)nc1C(=O)O
Reaction #71778
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)O
Reaction #71800
title compound
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCO[C@@H]1CN(c2nc(C(=O)O)c(C(=O)OCC)s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71807
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC(C)C(N)C(=O)NC[C@H]1OCC[C@H]1SC1=C(C(=O)O)N2C(=O)C(C(C)O)C2C1C
Reaction #83097
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc(C(=O)O)c2ccccc12
Reaction #84208
4-methoxy-1-naphthoic acid
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(C(=O)O)ccc21
Reaction #156133
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2cc(C)c(C(=O)O)s2)cc1
Reaction #156608
3-Methyl-5-p-tolylthiophene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C#N)(Cn1nc2cc(Cl)cc(C(=O)O)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158147
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1nc2cc(-n3ncc(C(=O)c4cc5ccccc5[nH]4)c3N)c(F)cc2[nH]1
Reaction #161619
[5-amino-1-(6-fluoro-2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl]-(1H-indol-2-yl)methanone
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cnc(Nc2ncnc3ccc(Oc4ncc(OCC(=O)O)cc4Cl)cc23)cn1
Reaction #168849
compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(-c2ccc(CC[C@@H](OC=O)[C@H](CCN3C(=O)c4ccccc4C3=O)C(=O)O)cc2)cn1
Reaction #171191
title compound
Ausbeute 221.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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