hypobromous acid

CC1Cc2cc(C(=O)O)ccc2O1
Reaction #3155
5-carboxy-2-methylcoumaran
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(C)CCOCCCCCCCCO
Reaction #64415
8-(3-methylpentyloxy)octanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1cc2ncnc(N3CCC(n4c(=O)c5cc(C(=O)O)ccc5n(C)c4=O)CC3)c2cc1OC
Reaction #83333
Compound 62
Ausbeute 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCCc1ccc(-c2ccc(C(=O)O)cc2)cc1
Reaction #415492
4'-n-pentyl-4-biphenylcarboxylic acid
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
NCCC(=O)[O-].NCCC(=O)[O-].[Mg+2]
Reaction #415743
Magnesium β-alaninate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CCC(C)CCOCCCCCCCCO
Reaction #526932
8-(3-methylpentyloxy)octanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
BrC1OC[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #670350
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
COc1cc2ncnc(N3CCC(n4c(=O)c5cc(C(=O)O)ccc5n(C)c4=O)CC3)c2cc1OC
Reaction #1234939
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
BrC1OC[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #1504362
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_03
COc1cc2ncnc(N3CCC(n4c(=O)c5cc(C(=O)O)ccc5n(C)c4=O)CC3)c2cc1OC
Reaction #1539099
Compound 62
Ausbeute 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
BrC1OC[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #1868449
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_05
COc1cc2ncnc(N3CCC(n4c(=O)c5cc(C(=O)O)ccc5n(C)c4=O)CC3)c2cc1OC
Reaction #2344933
Compound 62
Ausbeute 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_08