methyl 2,5-dihydroxybenzoate

COC(=O)c1cc(OCCC[Si](C)(C)C)ccc1O
Reaction #1162546
methyl 2-hydroxy-5-(3-trimethylsilanylpropyloxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_05
COC(=O)c1cc(OCCC[Si](C)(C)C)ccc1O
Reaction #1162862
methyl 2-hydroxy-5-(3-trimethylsilanylpropyloxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_05
COC(=O)c1cc(OCCCCCCc2cccc(OCc3ccccc3)c2OCc2ccccc2)ccc1O
Reaction #1234826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CCCCCCNC(=O)c1cc(O)ccc1O
Reaction #1324515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COC(=O)c1cc(OCCC[Si](C)(C)C)ccc1O
Reaction #1325404
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COC(=O)c1cc(OCCC[Si](C)(C)C)ccc1O
Reaction #1379202
methyl 2-hydroxy-5-(3-trimethylsilanylpropyloxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
COC(=O)c1cc(OCCCCCCc2cccc(OCc3ccccc3)c2OCc2ccccc2)ccc1O
Reaction #1581416
2-hydroxy-5-[6-[2,3-bis(phenylmethoxy)phenyl]hexyloxy]benzoic acid methyl ester
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_06
COC(=O)c1cc(OCc2ccccc2)ccc1O
Reaction #1584162
methyl 5-(benzyloxy)-2-hydroxybenzoate
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COC(=O)c1cc(OCCC[Si](C)(C)C)ccc1O
Reaction #1687666
methyl 2-hydroxy-5-(3-trimethylsilanylpropyloxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
COC(=O)c1cc(OCCCCCCc2cccc(OCc3ccccc3)c2OCc2ccccc2)ccc1O
Reaction #1700244
2-hydroxy-5-[6-[2,3-bis(phenylmethoxy)phenyl]hexyloxy]benzoic acid methyl ester
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_03
COC(=O)c1cc(OS(=O)(=O)c2ccc(C)cc2)ccc1O
Reaction #1710838
Methyl 2-hydroxy-5-{[(4-methylphenyl)sulfonyl]oxy}benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
COC(=O)c1cc(OS(=O)(=O)c2ccc(C)cc2)ccc1OCc1ccccc1
Reaction #1710840
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
COC(=O)c1cc(OS(=O)(=O)c2ccc(C)cc2)ccc1OCc1ccccc1
Reaction #1710841
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
COC(=O)c1cc(OCc2ccccc2)ccc1O
Reaction #1731762
methyl 5-benzyloxy-2-hydroxybenzoate
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
CCCCCCNC(=O)c1cc(O)ccc1O
Reaction #1833427
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
COC(=O)c1cc(OCc2ccccc2)ccc1O
Reaction #1833636
methyl 5-(benzyloxy)-2-hydroxybenzoate
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
COC(=O)c1cc(OCc2cccc(Cl)c2)ccc1O
Reaction #1856346
2-Carbomethoxy-4-(m-chlorophenylmethyloxy)-phenol
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
COC(=O)COc1ccc(OCC(=O)OC)c(C(=O)OC)c1
Reaction #2044995
4
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCCCCCNC(=O)c1cc(O)ccc1O
Reaction #2056344
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
COC(=O)c1cc(OCc2ccccc2)ccc1O
Reaction #2243584
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
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