zinc sulfate

COc1cnc2ccc(Cc3nnc4ccc(-c5cc(C)ns5)nn34)cc2c1
Reaction #68680
3-methoxy-6-((6-(3-methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline
Rendimiento 1.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=P(O)(O)CN(CCN(CP(=O)(O)O)CP(=O)(O)O)CP(=O)(O)O
Reaction #215334
EDTMP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COc1cnc2ccc(Cc3nnc4ccc(-c5cc(C)ns5)nn34)cc2c1
Reaction #306455
3-methoxy-6-((6-(3-methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline
Rendimiento 1.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=S(=O)([O-])[O-].[NH4+].[NH4+]
Reaction #498281
ammonium sulfate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
[O-]n1ccccc1=S.[O-]n1ccccc1=S.[Zn+2]
Reaction #937563
zinc pyrithione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
[O-]n1ccccc1=S.[O-]n1ccccc1=S.[Zn+2]
Reaction #937564
zinc pyrithione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
[O-]n1ccccc1=S.[O-]n1ccccc1=S.[Zn+2]
Reaction #937565
zinc pyrithione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
CCCCCCCCCCCCCCCCCCOP(=O)([O-])[O-].[Zn+2]
Reaction #1059230
zinc stearyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_07
[O-]n1ccccc1=S.[O-]n1ccccc1=S.[Zn+2]
Reaction #1078573
zinc pyrithione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_10
O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.[Zn+2]
Reaction #1106454
zinc picolinate
Rendimiento 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O.O=S(=O)([O-])O.[Cl-].[Zn+2]
Reaction #1162620
glucosamine sulfate zinc chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_05
N[C@@H](Cc1ccccc1)C(=O)[O-].N[C@@H](Cc1ccccc1)C(=O)[O-].[Zn+2]
Reaction #1175165
zinc phenylalaninate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Zn+2]
Reaction #1245774
zinc stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)[O-])C(=O)[O-].CCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)[O-])C(=O)[O-].CCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)[O-])C(=O)[O-].[Al+3].[Al+3]
Reaction #1265345
aluminum N-myristoyl-L-glutamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
O=C([O-])[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.O=C([O-])[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[Zn+2]
Reaction #1265346
zinc gluconate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
CC(O)C(=O)[O-].CC(O)C(=O)[O-].[Zn+2]
Reaction #1265348
zinc lactate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
COCOc1cc(COC)c(OCOC)c(C2=C(C(=O)OC)CCC2)c1
Reaction #1266649
subtitled product
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
[O-][n+]1ccccc1S.[Zn]
Reaction #1468470
Zinc Pyridine-2-thiol-N-oxide
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_04
[O-][n+]1ccccc1S.[Zn]
Reaction #1468471
Zinc Pyridine-2-thiol-N-Oxide
Rendimiento 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_04
CC[C@H](C)[C@H](N)C(=O)O
Reaction #1491505
Isoleucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
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