ethanol;hydrate

—
Reaction #1914
pure product
Rendimiento 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NN=Cc1ncccc1O)Nc1ccccc1
Reaction #1916
product
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCC(C)(C(=O)O)C(=O)O
Reaction #4268
2-Methyl-2-propargyl-malonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(O)c1cc2c(c(C(=O)O)c1)NCCCC2
Reaction #5029
compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cn(-c2cccc(C(F)(F)F)c2)c(=N)s1
Reaction #5418
2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline
Rendimiento 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1nc(SC)sc1C(=O)O
Reaction #5425
4-Ethoxycarbonyl-2-methylthiothiazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CSc1nc(C(=O)O)c(C(=O)NC(C)(C)C)s1
Reaction #5430
5-tert-Butylaminocarbonyl-2-methylthiothiazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Clc1ccc([C@@H]2CNc3ccccc3S2)cc1
Reaction #5935
(R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
Rendimiento 58.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Clc1ccc([C@@H]2CNc3c(ccc4ccccc34)S2)cc1
Reaction #5937
(R)-(+)-3-(4-chlorophenyl)- 2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine
Rendimiento 63.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc2nc(NC(=O)NCc3cccnc3)sc2c1
Reaction #9200
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCN1CN(C)CN(c2nc3ccc([N+](=O)[O-])cc3s2)C1=O
Reaction #9201
1-Ethyl-5-methyl-3-(6-nitro-1,3-benzothiazol-2-yl)-1,3,5-triazinan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCN1CN(C)CN(c2nc3c(s2)C(=O)CCC3)C1=O
Reaction #9251
pure product
Rendimiento 100.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #9658
solid
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)[C@@H]1C[C@H](SC(C)=O)CN1C
Reaction #10039
title compound
Rendimiento 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCc1c[nH]c2ccc(C(=O)OCC)cc12
Reaction #42489
title compound
Rendimiento 7.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)C1(CN2CCC(=O)CC2)CCOCC1
Reaction #44855
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cccc(CCc2cc(NC(=O)c3ccc(C(N)=O)cc3)[nH]n2)c1
Reaction #45012
solid
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCc1ccc(C(=O)O)c(O)c1
Reaction #46731
product
Rendimiento 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C(F)(F)F)CC(=O)c2cc(Br)ccc2O1
Reaction #48332
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CC(O)(c3ccccc3)CN2)c1
Reaction #49236
title compound
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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