Substructure Search

19540

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
O=C(O)CC1C2CCC1CC2
Reaction #47636
bicyclo[2.2.1]hept-7-yl-acetic acid
Yield 63.0%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
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54066
title compound
Yield 25.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C#CC1CCCCC1Cl
Reaction #54842
3-chloro-4-cyclohexylpropiolic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C#CC1CCCCC1Cl
Reaction #54843
propiolic acid
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
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Br)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57408
α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Br)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57409
α-bromo-3-hydroxytricyclo [3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57410
a-amino-3-hydroxytricyclo[3.3.1.1 3,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Br)C12CC3CC(CC(C3)C1)C2
Reaction #57413
α-bromotricyclo[3.3.1.13,7]decane-1-acetic acid
Yield 66.0%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)c1cccc2c1c1c(n2CC2CCCCC2)CCCC1=O
Reaction #79729
9-[(cyclohexyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one
Yield 97.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(CC1CCCCC1)c1ccccn1
Reaction #80846
1-(R,S)-(2-pyridyl)-2-cyclohexylethylamine
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(CC1CCCCC1)c1ccccn1
Reaction #80847
1-(R,S)-(2-pyridyl)-2-cyclohexylethylamine
Yield 43.5%DOI: 10.6084/m9.figshare.5104873.v1
NC(CC1CCCCC1)c1ccccn1
Reaction #80849
racemic 1-(2-pyridyl)-2-cyclohexylethylamine
Yield 45.0%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
O=C(OCC1CCCCC1)c1ccc(Br)o1
Reaction #91599
cyclohexylmethyl 5-bromofuran-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc([N+](=O)[O-])c(OCC2CCCCC2)c1
Reaction #92675
3-(cyclohexylmethoxy)-5-methyl-2-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next