2-(1,3-benzodioxol-5-yl)acetic acid

c1csc(-c2nn3c(Cc4ccc5c(c4)OCO5)nnc3s2)c1
Reaction #40720
compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CCNC(=O)Cc2ccc3c(c2)OCO3)cc1OC
Reaction #76861
N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-3,4-methylenedioxyphenyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(Cc1ccc2c(c1)OCO2)NC1CCC(CCN2CCC(c3cccc4c3OCO4)CC2)CC1
Reaction #211002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cc1ccc2c(c1)OCO2)NC1CCC(CCN2CCN(c3nccc4c3OCC4)CC2)CC1
Reaction #255943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cc1ccc2c(c1)OCO2)NN=Cc1ccccc1OS(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #268233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)Cc1ccc2c(c1)OCO2
Reaction #362108
methyl (3,4-methylenedioxyphenyl)acetate
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COC(=O)Cc1ccc2c(c1)OCO2
Reaction #377479
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OCCc1ccc2c(c1)OCO2
Reaction #378870
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Cc1ccc2c(c1)OCO2)Nc1cc(C2CC2)n[nH]1
Reaction #411750
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C(Cc1ccc2c(c1)OCO2)N[C@H]1CC[C@H](CCN2CCC(c3cccc4c3CCO4)CC2)CC1
Reaction #418676
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
OCCc1ccc2c(c1)OCO2
Reaction #462758
title compound
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
O=C(O)Cc1ccccc1
Reaction #487062
Phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
O=C(O)Cc1c[nH]c2ccccc12
Reaction #487065
3-Indolylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
COC(=O)Cc1ccc2c(c1)OCO2
Reaction #529838
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
OCCc1ccc2c(c1)OCO2
Reaction #543768
oil
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
O=C(Cc1ccc2c(c1)OCO2)Nn1nc(-c2ccc(Cl)cc2)c2ccccc2c1=O
Reaction #556858
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
OCCc1ccc2c(c1)OCO2
Reaction #571507
title compound
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
O=C(Cc1ccc2c(c1)OCO2)Nn1nc(N2CCOCC2)c2ccccc2c1=O
Reaction #622777
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C(Cl)Cc1ccc2c(c1)OCO2
Reaction #704361
3,4-methylenedioxyphenylacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
OCCc1ccc2c(c1)OCO2
Reaction #834451
2-benzo[1,3]dioxol-5-yl-ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
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