cyclohexanecarboxamide

NC(=S)C1CCCCC1
Reaction #160780
cyclohexanecarbothioamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NCN1CCN(c2ccccn2)CC1)C1CCCCC1
Reaction #298199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=S)C1CCCCC1
Reaction #326629
cyclohexanecarbothioamide
المردود 78.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
ClCc1coc(C2CCCCC2)n1
Reaction #409449
4-chloromethyl-2-cyclohexyloxazole
المردود 2.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C(NCN1CC=C(c2ccccn2)CC1)C1CCCCC1
Reaction #577358
pure compound
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(NCN1CCN(c2ccccn2)CC1)C1CCCCC1
Reaction #577368
pure compound
المردود 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(NC(O)C(Cl)(Cl)Cl)C1CCCCC1
Reaction #583780
cyclohexyl-N-(2,2,2-trichloro-1-hydroxyethyl)carboxamide
المردود 80.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
NC(=S)C1CCCCC1
Reaction #677401
cyclohexanecarbothioamide
المردود 78.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1cccc(C23CCC(=O)C(C2)NC3=O)c1
Reaction #911997
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2nc(-c3ccnc(-c4ccc5nc(NC(=O)C6CCCCC6)ccc5c4)c3)sc2c1-c1ccc(Cl)cc1
Reaction #966560
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CCOC(=O)c1sc(C2CCCCC2)nc1C
Reaction #1004568
ethyl 2-cyclohexyl-4-methylthiazole-5-carboxylate
المردود 184.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
O=C(NCN1CCC(c2ccccn2)CC1)C1CCCCC1
Reaction #1029615
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
NC(=S)C1CCCCC1
Reaction #1038684
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C(Nc1cncnc1)C1CCCCC1
Reaction #1071755
title compound
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
O=C(NCN1CC=C(c2ccccn2)CC1)C1CCCCC1
Reaction #1199995
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(Nc1cncnc1)C1CCCCC1
Reaction #1330165
title compound
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
—
Reaction #1667310
( 5 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_01
NC(=S)C1CCCCC1
Reaction #1758299
cyclohexanecarbothioamide
المردود 78.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
CC(C)[C@H]1COC(=O)N1c1ccnc(N(C(=O)OC(C)(C)C)[C@@H](C)c2ccc(NC(=O)C3CCCCC3)cc2)n1
Reaction #1937311
solid
المردود 58.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
O=C(Nc1cncnc1)C1CCCCC1
Reaction #1970518
title compound
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_07
الصفحة 1التالي