H3PO4

CCCCCCCCCCCCCCOCC(O)CNCCOP(=O)([O-])O.[Na+]
Reaction #1202
title compound
Rendimiento 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc(-c2ccc(Cl)cc2)c[nH]1
Reaction #1602
5-(4-chlorophenyl)-2-pyridinone
Rendimiento 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc(-c2ccc(Cl)cc2)c[nH]1
Reaction #1669
5-(4-chlorophenyl)-2-pyridinone
Rendimiento 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc(-c2ccc(Cl)cc2)c[nH]1
Reaction #2174
5-(4-chlorophenyl)-2-pyridinone
Rendimiento 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc(-c2ccc(Cl)cc2)c[nH]1
Reaction #2215
5-(4-chlorophenyl)-2-pyridinone
Rendimiento 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc(-c2ccc(Cl)cc2)c[nH]1
Reaction #2273
5-(4-chlorophenyl)-2-pyridinone
Rendimiento 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P([O-])([O-])OP(=O)([O-])[O-].[Ti+4]
Reaction #3152
titanium pyrophosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P([O-])([O-])OP(=O)([O-])[O-].[Ti+4]
Reaction #3153
titanium pyrophosphate
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
Reaction #3844
P2O5
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1ccc(O)cc1O
Reaction #4978
product
Rendimiento 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(O)c(C)c1O
Reaction #4981
solid
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(OC)nc(Oc2cccc(-c3cc[nH]n3)c2C(=O)ON(C)C)n1
Reaction #5910
6-Pyrazolyl-2-(4,6-dimethoxypyrimidin-2-yloxy)-1-(N,N-dimethylaminooxycarbonyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CON1CN(OC)CN(Oc2cccc(-c3ncc[nH]3)c2C(=O)On2cccn2)C1
Reaction #5911
6-Imidazolyl-2-(3,5-dimethoxy-s-triazin-1-yloxy)-1-[(1-pyrazolyl)-oxycarbonyl]-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=Cc1ccc(OC(C)=O)cc1
Reaction #6377
4-acetoxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC1(C)CCSc2ccccc21
Reaction #6629
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1ccc(CCl)c2ccccc12
Reaction #8301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc(C(=O)c2sc(Nc3ccc(N4CCN(C(C)C)CC4)cc3)nc2N)c1.O=P(O)(O)O
Reaction #10908
{4-Amino-2-[4-(4-isopropyl-piperazin-1-yl)-phenylamino]-thiazol-5-yl}-(3-methoxy-phenyl)-methanone; compound with phosphoric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NC(=O)N[C@@H](Cc1ccccc1)C(=O)O
Reaction #11299
N-carbamylphenylalanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=P(O)(O)O
Reaction #43886
oseltamivir phosphate
Rendimiento 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[SiH2]OC(C)(C)C1CC(=O)N(C2CCCCCC2)C1
Reaction #44478
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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