triethanolamine

COS(=O)(=O)[O-].[NH3+]CCO
Reaction #52143
N-(2-hydroxyethyl)ammonium methyl sulfate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C([O-])c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-].OCC[NH+](CCO)CCO
Reaction #55599
Tris-(2-hydroxyethyl)ammonium 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)/C=C\C(=O)O.OCCN(CCO)CCO
Reaction #76110
Triethanolamine Maleic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C([O-])c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-].OCC[NH+](CCO)CCO
Reaction #93611
Tris-(2-hydroxyethyl)ammonium 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCOC(=O)Nc1ccccc1N1CC2(CCN(C)CC2)c2ccccc21
Reaction #95504
1-[2-(ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC12CCC(=O)C(CSc3ccccc3)=C1CCC1C2CCC2(C)C(=O)CC(O)C12
Reaction #175320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(CNC(=O)c1ccccc1)C(C)O
Reaction #177668
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)CCC(=O)c1ccccc1
Reaction #185835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1nc(C(=O)O)ccc1CN1CC1C#N
Reaction #200420
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C([O-])CCCCC1SCC2NC(=O)NC21
Reaction #200713
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CCNC(C)CO)cc1OC
Reaction #202290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #206296
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCn1c(C)c(-c2c(S(C)(=O)=O)ccc(C)c2-c2ccc(N(C)C)cc2)c2ccccc21
Reaction #215058
[(4-dimethylaminophenyl)(1-ethyl-2-methyl-3-indolyl)(4-methylphenylsulfonyl)]methane
收率 83.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
—
Reaction #217152
bistriethanolamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Nc1ccccc1C(=O)O.Nc1ccccc1C(=O)O.Nc1ccccc1C(=O)O.OCCN(CCO)CCO
Reaction #217450
beige solid
收率 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Oc1ccc2c(c1)CC(NCC(O)c1ccc(OCc3ccccc3)c(CCOCc3ccccc3)c1)CC2
Reaction #237153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C[SiH](C)OC(=O)c1ccccc1O
Reaction #265902
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)CCC(=O)NCCS
Reaction #273888
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCc1c(OCC(O)COc2cccc(NC(=O)c3nnn[nH]3)c2C#N)ccc(C(C)=O)c1O
Reaction #296122
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)O.OCCN(CCO)CCO
Reaction #328653
triethanolamine acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
第 1 页下一页