lactic acid

CC(O)C(=O)NCCNC(=O)C(C)O
Reaction #1503
N,N'-1,2-ethanediylbislactamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(O)C(=O)O.NC(=O)c1ccncc1
Reaction #10215
Isonicotinic Acid Amide Lactic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(CN2CCN(C(=O)[C@H](C)O)CC2)sc2c(N3CCOCC3)nc(Cl)nc12
Reaction #70176
(S)-1-(4-((2-chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(O)C(=O)O.O=C(O)CO
Reaction #93377
lactic acid glycolic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(O)C(=O)O.CC(O)C(=O)O.CC(O)CNCCNc1ccc(NCCNCC(C)O)c2c1C(=O)c1c(O)ccc(O)c1C2=O
Reaction #93678
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
COc1ccc(COC(=O)C(C)O)cc1
Reaction #183160
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)C(=O)O
Reaction #187005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)C(=O)O
Reaction #194414
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)C(=O)N(C)CCOc1cccc2ncnc(Nc3ccc(OCc4ccccn4)c(Cl)c3)c12
Reaction #194567
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OC(C)C(=O)O
Reaction #199067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)C(=O)OC(=O)C(C)O
Reaction #211497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCNc1ccc(C(=O)OC(C)C(=O)O)cc1
Reaction #214122
1-carboxyethyl 4-(hexadecylamino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
C=C(C)c1c(OC)cc(Cc2cnc(N)nc2N)cc1OC.CC(O)C(=O)O
Reaction #214207
2,4-diamino-5-(4-isopropenyl-3,5-dimethoxybenzyl)-pyrimidine lactate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Cc1ccc(S(=O)(=O)OC[C@@H]2NC(=O)[C@@H]2NC(=O)OC(C)(C)C)cc1
Reaction #215081
crystalline title product
Ausbeute 71.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CC(OC(=O)Cc1ccc(NCCC2CCCCC2)cc1)C(=O)O
Reaction #215519
1-carboxyethyl 4-(2-cyclohexylethylamino)-phenylacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCN(CC)CCN1CCc2[nH]c(C=C3C(=O)Nc4ccc(F)cc43)c(C)c2C1=O
Reaction #223344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)Cn1c(N2CCN(C(=O)C(C)O)CC2)nc2c(N3CCOCC3C)nc(-c3cnc(N)nc3)nc21
Reaction #224780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O)C(=O)NCCOCCO
Reaction #229048
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1nc(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(C)CC4)ccc3OCC)nn12
Reaction #229979
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ncc(Br)cc1NC(=O)C(C)O
Reaction #238683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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