2-(2-chloroethoxy)ethanol

O=C(O)CN1CCN(CCOCCO)CCN(CC(=O)O)CCN(CC(=O)O)CC1
Reaction #65328
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C1c2ccccc2C(=O)N1CCOCCO
Reaction #173927
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCOCCN1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #190297
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)OCCOCCCl
Reaction #233459
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCOCCN1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #290292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1ccc(O)cc1)c1ccc(OCCOCCO)cc1
Reaction #316355
compound 61
Выход 45.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1ccccc1-c1cc(N2CCN(CCOCCO)CC2)ncc1C(=O)N(C)Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #368630
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccccc1-c1cc(N2CCN(CCOCCO)CC2)ncc1C(=O)N(C)Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #466579
title compound
Выход 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
O=C1c2ccccc2C(=O)N1CCOCCO
Reaction #486761
compound 15
Выход 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
Cc1ccc(S(=O)(=O)OCCOCCCl)cc1
Reaction #518613
2-(2-chloroethoxy)ethyl p-toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
OCCOCCN1CCOCC1
Reaction #541245
2-(2-morpholinoethoxy)ethanol
Выход 34.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
OCCOCCN1CCOCC1
Reaction #541300
2-(2-morpholinoethoxy)ethanol
Выход 34.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)c1ccc(OCCOCCO)cc1
Reaction #541968
ethyl 4-(2-(2-hydroxyethoxy)-ethoxy)benzoate
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
OCCOCCN1CCOCC1
Reaction #634396
2-(2-morpholinoethoxy)ethanol
Выход 34.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
OCCOCCSCCOCCO
Reaction #667490
1,11-dihydroxy-3,9-dioxa-6-thiaundecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_06
Cc1ccc(C[C@@H]2CN(CCOCCO)CCN2C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1C
Reaction #671366
(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[2-(2-hydroxyethoxy)ethyl]piperazine
Выход 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
OCCOCCNc1ccccc1OCCO
Reaction #698944
N-[2-(2-hydroxyethoxy)ethyl]-2-(2-hydroxyethoxy)aniline
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CS(=O)(=O)OCCOCCCl
Reaction #759426
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
OCCOCCN1CCCC1
Reaction #801388
2-(2-(pyrrolidin-1-yl)ethoxy)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
OCCOCCN1CC[C@H](F)C1
Reaction #801389
(S)-2-(2-(3-fluoropyrrolidin-1-yl)ethoxy)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
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