1-chloro-2-ethoxyethane

CCOCCOc1cccc([N+](=O)[O-])c1[N+](=O)[O-]
Reaction #46877
1-(2-Ethoxy-ethoxy)-2,3-dinitro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOCCn1c(CC)nc2ccccc21
Reaction #195389
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCn1c(C2CCN(C)CC2)nc2cccnc21
Reaction #291322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOCCOc1cc(C)c(Br)c(C)c1
Reaction #360566
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCOCCn1c(C)nc2ccccc21
Reaction #407177
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOCCn1c(NC2CCN(Cc3ccccc3)CC2)nc2ccccc21
Reaction #410362
(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-benzylpiperidin-4-yl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOCCn1c(Cl)nc2ccccc21
Reaction #410364
1-(2-ethoxyethyl)-2-chloro-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOCCn1c(NC2CCN(CCC3(c4ccc(C)c(C)c4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #410412
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCCC(=O)OC.CCN(CC)CC
Reaction #410416
methanol ethyl acetate triethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOCCn1c(NC2CCN(CCC3(Cc4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #410455
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOCCN1CCC(Nc2nc3cccnc3n2Cc2ccoc2C)CC1.O.O
Reaction #417726
N-[1-(2-ethoxyethyl)-4-piperidinyl]-3-[(2-methyl-3-furanyl)methyl]-3H-imidazo-[4,5-b]pyridin-2-amine dihydrate
المردود 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CCOCCn1c(C(=O)C2CCN(CCC(CN(C)C(=O)c3ccccc3)c3ccc(Cl)c(Cl)c3)CC2)nc2ccccc21
Reaction #466638
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCOCCn1c(C(=O)C2CCN(CCC(CN(C)C(=O)c3cc(OC)c(OC)c(OC)c3)c3cccc(Cl)c3)CC2)nc2ccccc21
Reaction #466651
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCOCCn1c(C(=O)C2CCN(CCC(CN(C)C(=O)c3cc(OC)c(OC)c(OC)c3)c3ccc(Cl)cc3)CC2)nc2ccccc21
Reaction #466653
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCOCCOc1cc(C)c(Br)c(C)c1
Reaction #532293
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOCCSc1nc2cc(Cl)ccc2s1
Reaction #574325
desired compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CCCOCCOc1cc2c(-c3ccccc3)c(CC(=O)Nc3ccc(Cl)cc3C(F)(F)F)c(=O)oc2cc1Cl
Reaction #576054
title compound
المردود 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
CCOCCOc1cc(C)c(-c2cccc(C=O)c2)c(C)c1
Reaction #595096
title compound
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCOCCn1c(-c2ccccc2)c(Br)c2ccccc21
Reaction #595101
title compound
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCOCCOc1ccc(-c2cc(C(=O)OC)ccc2OCc2ccccc2)cc1
Reaction #595117
title compound
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
الصفحة 1التالي