cyclohexanol

CC1(C)CCC(OC2CCCCC2)c2cc(Br)ccc21
Reaction #1311
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CO[Si](OC)(OC1CCCCC1)C1CCCC1
Reaction #6542
cyclohexyloxy cyclopentyl dimethoxysilane
収率 83.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #10042
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COC1CCCCC1
Reaction #47088
product 407
収率 887.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(S(=O)(=O)OC2CCCCC2)cc1
Reaction #49768
cyclohexyl p-toluenesulfonate
収率 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
C[C@]12CC[C@@H]3c4ccc(OC(=O)c5ccccc5)cc4CC[C@H]3[C@@H]1CC[C@@H]2O
Reaction #51282
Estradiol Benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc2cc(OC3CCCCC3)cnc2cc1OC
Reaction #51615
3-Cyclohexyloxy-6,7-dimethoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc2ncc(OC3CCCCC3)nc2cc1OC1CCCCC1
Reaction #51621
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1c2ccccc2C(=O)N1OC1CCCCC1
Reaction #57478
2-(cyclohexyloxy)-1H-isoindole-1,3(2H)-dione
収率 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC1(O)CCCCC1
Reaction #59841
Methoxycyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1cc2c(Cl)ncnc2s1
Reaction #60793
title compound
収率 53.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1cnc(-c2ccccc2)c1-c1nc2c(N)ncnc2n1C1CCCCC1
Reaction #60824
title compound
収率 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CCl)OC1CCCCC1
Reaction #62571
cyclohexyl chloroacetate
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
N=C(OC1CCCCC1)N1Cc2ccccc2-c2ccccc2C1
Reaction #63446
cyclohexyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboximidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
N=C(OC1CCCCC1)N1Cc2ccccc2-c2ccccc2C1
Reaction #63447
cyclohexyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboximidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C(O)C(C(=O)OC1CCCCC1)c1ccccc1
Reaction #65181
cyclohexyl hydrogen phenylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(Nc1ccccc1)N1CCN(Cc2ccc(OC3CCCCC3)cc2)CC1
Reaction #68869
title compound
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc(NC2CCCCC2)cc1
Reaction #81092
N-cyclohexylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)C(C(=O)OC1CCCCC1)c1ccccc1
Reaction #81476
cyclohexyl hydrogen phenylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)COC1CCCCC1
Reaction #84542
title compound
収率 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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