6-hydroxycoumarin

O=c1ccc2cc(OCCBr)ccc2o1
Reaction #262206
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=c1ccc2cc(OCCBr)ccc2o1
Reaction #463570
product
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOC(=O)CCCCOc1ccc2oc(=O)ccc2c1
Reaction #553136
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
O=c1ccc2cc(OC3CCC4(CCNCC4)CC3)ccc2o1
Reaction #641657
6-(3-Aza-spiro[5.5]undec-9-yloxy)-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCOC(=O)CCCCOc1ccc2oc(=O)ccc2c1
Reaction #698877
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
COCOc1ccc2oc(=O)ccc2c1
Reaction #819491
6-methoxymethoxy coumarin
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CC(C)=CCOc1ccc2oc(=O)ccc2c1
Reaction #1138216
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CC(C)=CCC/C(C)=C/COc1ccc2oc(=O)ccc2c1
Reaction #1138217
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CC(C)=CCC/C(C)=C/CC/C(C)=C/COc1ccc2oc(=O)ccc2c1
Reaction #1138218
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CC(C)=CCC/C(C)=C/CC/C(C)=C/CC/C(C)=C/COc1ccc2oc(=O)ccc2c1
Reaction #1138219
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
COCOc1ccc2oc(=O)ccc2c1
Reaction #1264005
6-methoxymethoxy coumarin
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
O=c1ccc2cc(OCCBr)ccc2o1
Reaction #1504129
product
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
CC(C)=CCOc1ccc2oc(=O)ccc2c1
Reaction #1564460
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CC(C)=CCC/C(C)=C/COc1ccc2oc(=O)ccc2c1
Reaction #1564461
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CC(C)=CCC/C(C)=C/CC/C(C)=C/COc1ccc2oc(=O)ccc2c1
Reaction #1564462
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CC(C)=CCC/C(C)=C/CC/C(C)=C/CC/C(C)=C/COc1ccc2oc(=O)ccc2c1
Reaction #1564463
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CC(C)CCCC(C)CCOc1ccc2oc(=O)ccc2c1
Reaction #1564464
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CCOC(=O)CCCCOc1ccc2oc(=O)ccc2c1
Reaction #1621127
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_02
CCOC(=O)CCCCOc1ccc2oc(=O)ccc2c1
Reaction #1744231
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_10
C=Cc1ccc(O)cc1
Reaction #1973947
4-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
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