4-bromophenol

CN1CCN(c2ccc(O)cc2)CC1
Reaction #339
المردود 51.0%750 AstraZeneca ELN dataset
Oc1ccc(N2CCOCC2)cc1
Reaction #375
المردود 31.3%750 AstraZeneca ELN dataset
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(O)cc1
Reaction #760
المردود 0.0%750 AstraZeneca ELN dataset
CC(C)(C)[Si](C)(Cc1ccc(Br)cc1)O[Si](C)(Cc1ccc(Br)cc1)C(C)(C)C
Reaction #1133
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(-c2cccnc2)cc1
Reaction #5435
above compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Brc1ccc(OCc2ccccc2)cc1
Reaction #11297
4-benzyloxybromobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(Oc2ccc(Br)cc2)cc1
Reaction #44753
4-(4-bromophenoxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccccc1Oc1ccc(Br)cc1
Reaction #46010
4-bromophenoxy-1-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCC(C)(C)c1cc(Br)ccc1O
Reaction #50652
4-bromo-2-(1,1-dimethyldecyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)(C)c1cc(Br)ccc1O
Reaction #51276
2-tert-butyl-4-bromophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)=CC(=O)Oc1ccc(Br)cc1
Reaction #52370
title compound
المردود 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCCCCOc1ccc(Br)cc1
Reaction #65095
4-bromo-1-n-octyloxybenzene
المردود 63.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Brc1ccc(OCC2CC2)cc1
Reaction #68838
1-Bromo-4-cyclopropylmethoxybenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc(Oc2ccccn2)cc1
Reaction #68976
2-(4-bromo-phenoxy)pyridine
المردود 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)CCCCOc1ccc(Br)cc1
Reaction #76392
1-Bromo-4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)[C@@H]1C[C@H](Oc2ccc(Br)cc2)CN1C(=O)OC(C)(C)C
Reaction #78244
cis-1-(Boc)-4-(4-bromo-phenoxy)-L-proline methyl ester
المردود 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1[C@@H]2C[C@H](Oc3ccc(Br)cc3)CN2C(=O)N1c1cc(Cl)cc(Cl)c1
Reaction #78259
titled compound
المردود 6.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(C=Cc1ccccc1)Oc1ccc(Br)cc1
Reaction #78866
3-phenylacrylic acid 4-bromophenyl ester
المردود 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#Cc1ccccc1Oc1ccc(Br)cc1
Reaction #79763
2-(4-bromophenoxy)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CC(=O)Oc1ccc(Br)cc1
Reaction #79939
title compound
المردود 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
الصفحة 1التالي