ammonium sulfate

Cl.NCCCC[C@@H](N)C(=O)O
Reaction #891
D-lysine monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC1CCC(n2cc(C)c(=O)[nH]c2=O)O1
Reaction #1652
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCOC1=C(SCCCCCC(=O)O)[C@@H](/C=C/[C@@H](O)C[C@@H](C)CCCC)[C@H](O)C1
Reaction #3122
(11R,12S,13E,15S,17S)-9-butyloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoic acid
Ausbeute 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #8989
solid
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1C2=C(CCCC2)C2CCCCC12
Reaction #10583
1,2,3,4,4a,5,6,7,8,9a-decahydro-9H-fluoren-9-one
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1C2=C(CCC2)[C@H]2CCC[C@@H]12
Reaction #10585
cis-tricyclo [6.3.0.03,7] undec-1(8)-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[Si](C)(C)N(c1cc[nH]c(=O)n1)[Si](C)(C)C
Reaction #50278
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Cc1cc(CO)c2ccccc2n1
Reaction #53540
2-methyl-4-hydroxymethylquinoline
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N[C@@H](CCC(=O)O)C(=O)O
Reaction #58019
L-glutamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)O[C@H]1[C@@H](NC(=O)Cc2cccc3c2Cc2ccccc2-3)[C@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@@H]1n1cnc2c(Cl)ncnc21
Reaction #58428
7
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN1C(=O)OC(C)(C)c2cc(-c3cccc(Br)c3)ccc21
Reaction #79010
6-(3-bromophenyl)-1,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(O)c1cc(-c2cccc(F)c2)ccc1N
Reaction #79012
1-(4-amino-3′-fluoro[1,1′-biphenyl]-3-yl)ethanol
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=S(=O)([O-])[O-].[NH4+].[NH4+]
Reaction #83161
ammonium sulfate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1=CC(=NO)CC(C)C1
Reaction #93886
3,5-dimethylcyclohexenone oxime
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCOC(=O)c1nc(C)n(C2CCCC2)c1C
Reaction #162678
solid
Ausbeute 71.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #215551
2,3,5,6-tetrachloropyridine
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
[Co+2].[Mn+2].[Ni+2].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-]
Reaction #218247
nickel-manganese-cobalt hydroxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CN1CN(C)c2nc3n(Cc4ccc(F)cc4)c(=O)cc(O)n3c2C1=O
Reaction #318812
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
C[Si](C)(C)N(c1cc[nH]c(=O)n1)[Si](C)(C)C
Reaction #321281
bis-trimethylsilylcytosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
C[Si](C)(C)N(c1cc[nH]c(=O)n1)[Si](C)(C)C
Reaction #321284
bis-trimethylsilylcytosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
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