3-hydroxy-4-methoxybenzaldehyde

COc1ccc(C=O)cc1OC1CCCC1
Reaction #1014
title compound
المردود 89.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C=O)cc1OC1CC2CCC1C2
Reaction #64754
green/brown oil
المردود 87.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1ccc(C=O)cc1OC1CCCC1
Reaction #82869
title compound
المردود 89.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc(C=O)c(Br)c1O
Reaction #94830
2-bromo-3-hydroxy-4-methoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
C=CCOc1cc(C=O)ccc1OC
Reaction #176687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=O)cc1OCc1ccccc1
Reaction #179349
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=O)cc1OC(=O)CCCc1ccccc1
Reaction #180028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=O)cc1OC(=O)c1ccccc1
Reaction #183488
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CNCc1ccc(OC)c(O)c1
Reaction #196622
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCCOc1cc(C=O)ccc1OC
Reaction #201636
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=O)cc1OCCCCCCOCCCCc1ccccc1
Reaction #204786
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=O)cc1OCCCCCCCCCCCc1ccccc1
Reaction #207147
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CNc2cccc(-c3c(Cc4ccccc4)cnc4c(C(F)(F)F)cccc34)c2)cc1O
Reaction #212366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=O)c(Br)c1O
Reaction #218765
2-bromoisovanillin
المردود 45.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1ccc(CN2CCC(CNC(=O)CNC(=O)c3cccc(C(F)(F)F)c3)CC2)cc1O
Reaction #220784
1-[3-hydroxy-4-methoxybenzyl]-4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1ccc(C=O)cc1S(=O)(=O)N(C)C
Reaction #221576
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C=O)cc1OCCF
Reaction #222821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C=O)cc1OCCCCCCOCCCCCCc1ccccc1
Reaction #223324
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCOc1cc(C=O)ccc1OC
Reaction #228235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C=O)cc1OCCBr
Reaction #230396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
الصفحة 1التالي