#CCCCC(C)O

CCCCC(C)OS(C)(=O)=O
Reaction #79252
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCC(C)OS(C)(=O)=O
Reaction #263281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCC(C)Oc1nc(N)c2ncn(C3CCCCO3)c2n1
Reaction #268758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCC(C)OC(=O)CCC(=O)CN.Cl
Reaction #316651
1-methyl-pentyl 5-amino-4-oxopentanoate Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #367991
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #572701
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #707094
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
CCCCC(C)OC(=O)CCC(=O)CN
Reaction #913545
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #932115
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_07
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #938438
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_05
CCCC(O)CC
Reaction #978028
3-hexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1023247
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1162146
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_07
CCCCC(C)OC(=O)CCC(=O)CN.Cl
Reaction #1269178
2-Hexyl 5-amino-4-oxopentanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1336088
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_12
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1372014
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_01
CCCCC(C)OC(=O)CCC(=O)CN.Cl
Reaction #1438606
1-methyl-pentyl 5-amino-4-oxopentanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
CCCCC(C)OC(=O)CCC(=O)CN.Cl
Reaction #1699258
2-Hexyl 5-amino-4-oxopentanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
CCCCC(C)OC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1849239
desired compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_05
CCCCC(C)OS(C)(=O)=O
Reaction #1852032
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06
1 ページ次のページ