3-methyl-1,3-butane diol

Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #165701
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #199229
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(O)CCOS(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #238154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(O)CCOc1c(Br)cnn(-c2ccc(F)c(F)c2)c1=O
Reaction #280881
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #324625
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC1=NC(C)(C)CCO1
Reaction #400236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #400280
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCn1/c(=N/C(=O)c2cc(C(F)(F)F)ccc2OCCC(C)(C)O)sc2ccncc21
Reaction #427830
title compound
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(=O)OCCC(C)(C)O
Reaction #428043
3-Hydroxy-3-methylbutyl acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(O)CCOc1c(Br)cnn(-c2ccc(F)c(F)c2)c1=O
Reaction #469172
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #558625
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(O)CCOc1cccc([N+](=O)[O-])c1C#N
Reaction #558896
2-(3-hydroxy-3-methylbutoxy)-6-nitrobenzonitrile
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cn1c(C2(C)CC2)c/c(=N\C(=O)c2cc(C(F)(F)F)ccc2OCCC(C)(C)O)n1C[C@H]1CCCO1
Reaction #623912
title compound
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CC1=NC(C)(C)CCO1
Reaction #651431
2,4,4-trimethyl-5,6-dihydro-1,3 (4H)-oxazine
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #666574
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
Reaction #712872
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(O)CCOS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #766617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)(O)CCOc1cccc([N+](=O)[O-])c1C#N
Reaction #799033
2-(3-hydroxy-3-methylbutoxy)-6-nitrobenzonitrile
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCc1c(Cn2ccnc2-c2nccs2)nc2ccc(OCCC(C)(C)O)nn12
Reaction #892656
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(O)CCOc1c(Br)cnn(-c2ccc(F)c(F)c2)c1=O
Reaction #978592
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
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