4-bromo-1,2-dimethoxybenzene

COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #811
Yield 36.0%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #812
Yield 60.0%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #813
Yield 90.5%750 AstraZeneca ELN dataset
COc1ccc(C2CCC(OC)O2)cc1OC
Reaction #50760
2-(3,4-dimethoxyphenyl)-5-methoxytetrahydrofuran
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1cc(Br)c([N+](=O)[O-])cc1OC
Reaction #60496
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)c2ccc(Oc3ccc(Cl)cc3)cn2)cc1OC
Reaction #176803
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(Br)c([N+](=O)[O-])cc1OC
Reaction #185912
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(Br)c([N+](=O)[O-])cc1OC
Reaction #188019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(=O)c2ccncc2)cc1OC
Reaction #222495
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C#CCCO)cc1OC
Reaction #236835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C2CCC(OC)O2)cc1OC
Reaction #278505
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOc1ccc(-c2nc(C(O)c3ccc(OC)c(OC)c3)cs2)cc1OCC
Reaction #350764
2-(3,4-diethoxyphenyl)-4-[1-hydroxy-1-(3,4-dimethoxyphenyl)methyl]thiazole
Yield 48.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COC(=O)c1c[nH]c2cc(Cl)c(-c3ccc(OC)c(OC)c3)cc12
Reaction #425501
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
—
Reaction #453787
product
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COc1ccc(C(=O)c2ccncc2)cc1OC
Reaction #453806
4-(3,4-Dimethoxybenzoyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COc1cc2ccc3c4cc(OC)c(OC)cc4ncc3c2cc1OC
Reaction #456940
2,3,8,9-Tetramethoxybenzo[i]phenanthridine
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COc1cc(Br)c(C(=O)c2ccccc2)cc1OC
Reaction #549868
(2-bromo-4,5-dimethoxyphenyl)-phenylmethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
COc1ccc(N2CCC(=CC#N)CC2)cc1OC
Reaction #608377
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
—
Reaction #670629
product
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
COc1ccc(C(=O)c2ccncc2)cc1OC
Reaction #670648
4-(3,4-Dimethoxybenzoyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
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