methyl 2,5-dihydroxybenzoate

COC(=O)c1cc(OCCC(C)CC(C)(C)C)ccc1O
Reaction #250797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOc1ccc(O)c(C(=O)OC)c1
Reaction #254685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCOc1ccc(O)c(C(=O)OC)c1
Reaction #262198
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(OCCCCCCCCCCCCOc2ccccc2)ccc1O
Reaction #275439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(OCCC(C)CC(C)(C)C)ccc1O
Reaction #351532
methyl 5-(3,5,5-trimethylhexyloxy)-2-hydroxybenzoate
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COC(=O)c1cc(OCCC2CCCCC2)ccc1O
Reaction #351533
methyl 5-(2-cyclohexylethoxy)-2-hydroxybenzoate
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCCOc1ccc(O)c(C(=O)OC)c1
Reaction #351534
methyl 5-n-hexyloxy-2-hydroxybenzoate
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCCCCCCCCCCCCCCOc1ccc(O)c(C(=O)OC)c1
Reaction #575470
2-hydroxy-5-(octadecyloxy)benzoic acid methyl ester
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CCCCCCCCCCCCCCOc1ccc(O)c(C(=O)OC)c1
Reaction #575489
hydroxy-5-(tetradecyloxy)benzoic acid methyl ester
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CCCCCCCCCCOc1ccc(O)c(C(=O)OC)c1
Reaction #575494
5-(decyloxy)-2-hydroxybenzoic acid methyl ester
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
COC(=O)c1cc(OCCCCCCOc2ccc(-c3ccccc3)cc2)ccc1O
Reaction #575504
5-[[6-([1,1'-biphenyl]4-yloxy)hexyl]oxy]-2-hydroxybenzoic acid methyl ester
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
COC(=O)c1cc(OCCCCCCCCCCCCOc2ccccc2)ccc1O
Reaction #575509
2-hydroxy-5-[(12-phenoxydodecyl)oxy]benzoic acid methyl ester
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
COC(=O)c1cc(OCc2ccccc2)ccc1O
Reaction #702000
methyl 5-benzyloxysalicylate
Выход 41.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_03
COC(=O)c1cc(O[Si](C)(C)C(C)(C)C)ccc1O
Reaction #724399
methyl 2-hydroxy-5-(t-butyldimethylsilyloxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
COC(=O)COc1ccc(OCC(=O)OC)c(C(=O)OC)c1
Reaction #725880
4
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)c1cc(OCCCCCCOc2ccc(-c3ccccc3)cc2)ccc1O
Reaction #765120
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cc(OCCCCCCc2cccc(OCc3ccccc3)c2OCc2ccccc2)ccc1O
Reaction #916794
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1ccc(OCCC[Si](C)(C)C)cc1O
Reaction #930461
methyl 2-hydroxy-4-(3-trimethylsilanyl-propyloxy)-benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
COC(=O)c1cc(O[Si](C)(C)C(C)(C)C)ccc1O
Reaction #1021899
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1cc(OCCC2CCCCC2)ccc1O
Reaction #1031306
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
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