m-cresol

Cc1cccc(O)c1C=O
Reaction #883
m-cresol formaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C#N)c(O)c1
Reaction #9011
2-Hydroxy-4-methylbenzonitrile
المردود 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCC[C@H](NC(=O)c1ccc(CNCc2ccccn2)s1)C(=O)O
Reaction #11948
title compound
المردود 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(OC[C@H](COCc2ccccc2)NC(=O)OC(C)(C)C)c1
Reaction #40680
t-butyl (1S)-2-(benzyloxy)-1-[(3-methylphenoxy)methyl]ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSC[C@@H](COc1cccc(F)c1)NC(=O)OC(C)(C)C
Reaction #40690
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)/C=C(\C)Oc1cccc(C)c1
Reaction #47557
(E)-3-m-tolyloxy-but-2-enoic acid ethyl ester
المردود 63.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(C=O)c(O)c1
Reaction #51206
title product
المردود 25.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(-c2nc(-c3ccc(Oc4ccccc4)cc3)nc(-c3ccc(Oc4ccccc4)cc3)n2)c(O)c1
Reaction #52129
2-(2-hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(-c2nc(-c3ccc(Oc4ccccc4)cc3)nc(-c3ccc(Oc4ccccc4)cc3)n2)c(O)c1
Reaction #52130
2-(2-hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cl.N=C(N)Nc1c(Cl)cccc1Cl
Reaction #55469
2,6-dichlorophenylguanidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CN(C(=N)N)c1c(Cl)cccc1Cl.Cl
Reaction #55471
1-(2,6-dichlorophenyl)-1-methylguanidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CNC(=N)Nc1c(Cl)cccc1Cl.Cl
Reaction #55473
1-(2,6-dichlorophenyl)-3-methylguanidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1cccc(O)c1C=O
Reaction #65310
m-cresolformaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cccc(O)c1-c1cccc(O)c1C=O
Reaction #65312
m-cresol-salicylaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cccc(OC2CCN(C(=O)OC(C)(C)C)C2)c1
Reaction #159597
title compound ( D38 )
المردود 107.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C=C(C)Oc1cccc(C)c1
Reaction #173016
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(OCC(=O)c2ccccc2)c1
Reaction #184273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(-c2ccccc2NC(=N)N2CCCCC2)c1
Reaction #188167
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2ccccc2)c(NC(=N)N2CCOCC2)c1
Reaction #200923
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-c2ccccc2NC(=N)N(C)C)cc1
Reaction #201273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي