部分構造検索

CCCC(C)CBr

O=C1Nc2ccccc2C12CCCC2Br
Reaction #7092
subtitled compound
収率 105.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C12CCCC2B(O)O
Reaction #7108
subtitled compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(CC2CCCC2)c1=O
Reaction #8098
title compound
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccccc2-c2ccc3c(c2)C2(c4cc(-c5ccccc5-c5ccccc5)ccc4-c4c(-c5ccccc5-c5ccccc5)cc(-c5ccccc5-c5ccccc5)cc42)c2cc(-c4ccccc4-c4ccccc4)cc(-c4ccccc4-c4ccccc4)c2-3)cc1
Reaction #8644
2,2′,4,4′,7,7′-hexabiphenylyl-9,9′-spirobifluorene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C12CCCC2Br
Reaction #9415
subtitled compound
収率 105.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(COCC4CCCCC4)nc3N21
Reaction #12036
(4R,9aR)-6-Cyclohexylmethoxymethyl-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC(=O)C1Br
Reaction #40333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)(OCC)P(=O)(CC1CCCCC1)OCC
Reaction #50055
1,1-diethoxyethyl(cyclohexylmethyl)phosphinic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)COc1ccc(OC)cc1
Reaction #50161
1-methoxy-4-(2'-methylpentyloxy)benzene
収率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54066
title compound
収率 25.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)cc(-c2cc(Cl)ccc2OCC2CCCCC2)n1
Reaction #56930
4-chloro-6-(5-chloro-2-cyclohexylmethoxy-phenyl)-pyrimidin-2-ylamine
収率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OCC1CCCCC1
Reaction #57437
2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1nc(Nc2cccc(Cl)c2)ncc1COCC1CCCCC1
Reaction #67072
N-(3-chlorophenyl)-5-[(cyclohexylmethoxy)methyl]-4-(trifluoromethyl)pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2c1c1c(n2CC2CCCCC2)CCCC1=O
Reaction #79729
9-[(cyclohexyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one
収率 97.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(CC1CCCCC1)c1ccccn1
Reaction #80846
1-(R,S)-(2-pyridyl)-2-cyclohexylethylamine
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(CC1CCCCC1)c1ccccn1
Reaction #80847
1-(R,S)-(2-pyridyl)-2-cyclohexylethylamine
収率 43.5%DOI: 10.6084/m9.figshare.5104873.v1
NC(CC1CCCCC1)c1ccccn1
Reaction #80849
racemic 1-(2-pyridyl)-2-cyclohexylethylamine
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(SC3COC(CO)C3)C(C)C12
Reaction #83062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1CCCCC1)c1ccc(Cl)s1
Reaction #91578
cyclohexylmethyl 5-chlorothiophene-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ