2-aminoethanol

CCCCCCC(O)CCCCCCCCCCCOCC(O)CNCCO
Reaction #1190
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)COCC(O)CNCCO
Reaction #1191
title compound
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC(CC)COCCCCCCCCCCOCC(O)CNCCO
Reaction #1194
title compound
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCOC(=O)CCCCCCCCCCCOCC(O)CNCCO
Reaction #1195
title compound
Ausbeute 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[Si](C)(C)CCCCCCCCCCCOCC(O)CNCCO
Reaction #1197
title compound
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCOCC(C)(O)CNCCO
Reaction #1199
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCOCC(O)CNCCOP(=O)([O-])O.[Na+]
Reaction #1202
title compound
Ausbeute 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1204
title compound
Ausbeute 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCOCC(NCCO)C(C)(C)O
Reaction #1206
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1209
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCCNCCCCCCCCCCCCCCCCOC1CCCCO1
Reaction #1212
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCSCC(O)CNCCO
Reaction #1213
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C=C(C)NCCO
Reaction #1351
XXIII
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(Oc2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCN)c1.Cl
Reaction #2363
Compound A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CSC(=S)N1CCO
Reaction #3038
desired subtitled intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1cc(NCCO)c(Cl)cc1[N+](=O)[O-]
Reaction #4333
2-amino-4-β-hydroxyethylamino-5-chloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NCCNc1cc(NCCO)c(Cl)cc1[N+](=O)[O-]
Reaction #4335
2-chloro-5-β-aminoethylamino-4-nitro-N-(β-hydroxyethyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Nc1cc(NCCO)c([N+](=O)[O-])cc1Br
Reaction #4336
2-β-hydroxyethylamino-4-amino-5-bromonitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(NCCO)NCc1ccccc1OCc1ccccc1
Reaction #4632
N-(2-hydroxyethyl)-N'-(2-benzyloxybenzyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1cc(CCO)c(NCCO)c([N+](=O)[O-])c1
Reaction #4853
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
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