phenol

COc1c(NOCc2ccccc2)ccnc1C
Reaction #1096
4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(Nc2ccc(C(C)(C)C)cc2)ccnc1C
Reaction #1106
4-(4-tert-Butylanilino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(Oc2ccccc2)ccc1[N+](=O)[O-]
Reaction #1841
2-Nitro-5-phenoxytoluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1c(Cl)c(Cl)c(Oc2ccccc2)c(Cl)c1C#N
Reaction #2726
3,5,6-Trichloro-1,2-dicyano-4-phenoxybenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1cc(C=O)ccc1O
Reaction #3050
3-(1,1-dimethylethyl)-4-hydroxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(O)c1ccc(O)cc1
Reaction #3145
phenolsulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(O)c1ccc(O)cc1
Reaction #3146
phenolsulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #4084
( I )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)c1ccccc1O.Oc1ccccc1
Reaction #4279
t-butyl phenol phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #4468
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #4469
2-(p-Nitrophenoxymethyl) quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)CCC(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
Reaction #4556
ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)c1cc(CO)c(O)c(CO)c1
Reaction #4789
4-tert-butyl-2,6-di(hydroxymethyl)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(c1ccccc1)c1ccc(O)c(C(C)(C)c2ccccc2)c1
Reaction #4810
2,4-Di-(alpha, alpha-dimethylbenzyl)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCCCCCCCCCCCCc1ccc(O)cc1
Reaction #5372
mono-hexadecylphenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Oc1ccc(-c2nnc(-c3ccc(O)cc3)n2-c2ccccc2)cc1
Reaction #5662
solid
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc(O)cc1
Reaction #5728
4-hydroxyacetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc(O)cc1
Reaction #5730
4-hydroxyacetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc(O)cc1
Reaction #5732
4-hydroxyacetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc(O)cc1
Reaction #5734
4-hydroxyacetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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