2,5-dimethylaniline

Cc1ccc(C)c(NC(=O)CC(=O)C(C)C)c1
Reaction #173219
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C)c(Nc2cc(C(F)(F)F)nc(-c3cccnc3)n2)c1
Reaction #195080
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(S(=O)(=O)O)c(C)cc1N
Reaction #214518
2,5-dimethyl-4-aminobenzenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Cc1ccc(C)c(NCc2cccc3[nH]nnc23)c1
Reaction #216004
N-(1-benzotriazolylmethyl)-2,5-dimethylaniline
Rendimiento 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(=O)Nc1cc(C)ccc1C
Reaction #363176
2′,5′-dimethylacetanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1ccc(C)c(Nc2ccccc2CC(=O)O)c1
Reaction #364399
2-[(2,5-dimethylphenyl)amino]phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc(C=O)c(C)cc1N
Reaction #384180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCC(C)C
Reaction #434917
isohexane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(=O)Nc1cc(C)ccc1C
Reaction #563114
2,5-Dimethylacetanilide
Rendimiento 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CO.Cc1cccc(N)c1C
Reaction #668633
xylidine methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
Cc1cc(Oc2snc(-c3ccccc3)c2Cl)c(C)cc1N
Reaction #766677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(=O)Nc1cc(C)ccc1C
Reaction #783103
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1ccc(C)c(NCc2cccc3[nH]nnc23)c1
Reaction #830336
N-(1-benzotriazolylmethyl)-2,5-dimethylaniline
Rendimiento 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
Cc1ccc(C)c(Nc2cc(C(F)(F)F)nc(-c3cnccn3)n2)c1
Reaction #1034084
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(=O)Nc1cc(CO)ccc1C
Reaction #1042476
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)N1CCC(CC(=O)Nc2cc(C)ccc2C)CC1
Reaction #1049379
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)c1cnc(Nc2cc(C)ccc2C)[nH]c1=O
Reaction #1066298
ethyl 1,6-dihydro-6-oxo-2-(2,5-dimethylanilino)-5-pyrimidinecarboxylate
Rendimiento 45.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
Cc1ccc2c(C)ccc(C)c2n1
Reaction #1074117
2,5,8-trimethylquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
Cc1cc(I)c(C)cc1N
Reaction #1104977
2,5-dimethyl-4-iodo-aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
CCOC(=O)c1cnn2c(Nc3cc(C)ccc3C)c(C(=O)N3CCC(c4ccccc4)CC3)cnc12
Reaction #1114188
title compound
Rendimiento 103.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
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