2-bromo-4-isopropyl-cyclohexanone

CC(C)C1CCc2nc(NC(=N)N)sc2C1
Reaction #40297
rac. N-(6-isopropyl-4,5,6,7-tetrahydro-benzothiazole-2-yl)-guanidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCC1CCC(Br)C(=O)C1
Reaction #40299
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CCC(=O)C(Br)C1
Reaction #40302
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CCCC(Br)C1=O
Reaction #40311
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC1(C)CCCC(Br)C1=O
Reaction #40313
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)CC1(C)CCCC(Br)C1=O
Reaction #40315
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC1(C)CCCC(Br)C1=O
Reaction #40317
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1CCCC(Br)C1=O
Reaction #40319
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1CCC(=O)C(Br)C1
Reaction #40322
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1C(Br)CCCC12CCCCC2
Reaction #40323
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCC(c2ccccc2)(c2ccccc2)CC1Br
Reaction #40325
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1(c2ccccc2)CCC(=O)C(Br)C1
Reaction #40326
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#CC1(c2ccccc2)CCC(=O)C(Br)C1
Reaction #40327
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CC(=O)C(Br)CC1c1ccccc1
Reaction #40331
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CC(c2ccccc2)CCCC1Br
Reaction #40334
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCC(=O)C(Br)C1
Reaction #40339
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CN(Cc2ccccc2)CCCC1Br
Reaction #40343
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1CCC(=O)C(Br)C1
Reaction #204551
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C(Br)CCCC12CCCCC2
Reaction #205632
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCC(c2ccccc2)(c2ccccc2)CC1Br
Reaction #231193
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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