cyclopentyl bromide

COc1ccc(C=O)cc1OC1CCCC1
Reaction #1014
title compound
收率 89.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(Cc2ccc(OC(C)C)cc2)c(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1C1CCCC1
Reaction #7491
1-cyclopentyl-3-(β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-1H-pyrazole
收率 58.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C#Cc2cn(C3CCCC3)c(C)n2)ccn1
Reaction #8975
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(C)=O)c(O)c1OC1CCCC1
Reaction #48903
1-[3-(cyclopentyloxy)-2-hydroxy-4-methoxyphenyl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49742
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 30.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)Nc1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49749
ethyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate
收率 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
—
Reaction #49751
4
收率 1388.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=c1ccc2cc(OC3CCCC3)c(O)cc2o1
Reaction #50639
6-(cyclopentyloxy)-7-hydroxy-2H-1-benzopyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Cc1ccc(C(C(=O)OC(C)(C)C)C2CCCC2)cc1
Reaction #53431
tert-Butyl 2-Cyclopentyl-2-(4-methylphenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(Cc1ccccc1)N(c1ccc(Cl)cc1)C1CCN(C2CCCC2)CC1
Reaction #55033
N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(O)C(c1cccc(Cl)c1)C1CCCCC1
Reaction #57105
(3-chlorophenyl)(cyclohexyl)acetic acid
收率 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1OC1CCCC1
Reaction #57429
2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dione
收率 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=Cc1ccc(OC2CCCC2)c(O)c1
Reaction #67610
4-cyclopentyloxy-3-hydroxy benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Ic1cc(I)c(OC2CCCC2)c(I)c1
Reaction #81768
amber oil
收率 107.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc(C=O)cc1OC1CCCC1
Reaction #82869
title compound
收率 89.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1ccc(Nc2nc3c(-c4cnn(C5CCCC5)c4)cccn3n2)cc1
Reaction #86048
solid
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1cc(Cl)c(OC2CCCC2)c(Cl)c1
Reaction #90990
methyl 3,5-dichloro-4-(cyclopentyloxy)benzoate
收率 84.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
FC(F)(F)c1ccccc1C1CCCC1
Reaction #91059
1-Cyclopentyl-2-(trifluoromethyl)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
FC(F)(F)c1ccccc1C1CCCC1
Reaction #91060
product
收率 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
FC(F)(F)c1ccccc1C1CCCC1
Reaction #91086
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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