Involved in 12 reactions

12474521

OCCCc1nc2cccnc2[nH]1
Reaction #443462
title compound
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CC[NH+](CC)CC.COc1ccc(C(OCCCC(=O)[O-])(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #499001
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
COc1ccc(C(OCCCC(=O)Oc2ccc([N+](=O)[O-])cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #983944
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_07
O=C(CCCO)OCc1ccccc1
Reaction #1290698
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCC(O)C(=O)O[C@@H]([C@H](O)[C@@H](O)CNC)[C@H](O)CO
Reaction #1378866
1-desoxy-1-methylamino-D-glucitol 4-hydroxybutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
NC(CO)(CO)CO.O=C(O)CCCO
Reaction #1378867
Trishydroxymethyl-aminomethane 4-hydroxybutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
OCCCc1nc2cccnc2[nH]1
Reaction #1686455
title compound
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_04
OCCCc1nc2cccnc2[nH]1
Reaction #1688993
title compound
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
CN1CCCC1=O
Reaction #1787142
NMP
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_02
COc1ccc(C(OCCCC(=O)Oc2ccc([N+](=O)[O-])cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #1810791
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
OCCCc1nc2cccnc2[nH]1
Reaction #1825398
title compound
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_10
OCCCc1nc2cccnc2[nH]1
Reaction #2040872
title compound
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_09