3-chloro-1,2-propanediol

O=[N+]([O-])c1cc(OCC(O)CO)c(OCC(O)CO)cc1[N+](=O)[O-]
Reaction #3194
light yellow fluffy solid
Ausbeute 67.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1cccc(C(F)(F)F)c1CC(O)CO
Reaction #62710
2,3-dihydroxypropyl-3-aminobenzotrifluoride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cn1cc[n+](CC(O)CO)c1.[Cl-]
Reaction #90824
product
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1n(C)cc[n+]1CC(O)CO.[Cl-]
Reaction #90825
solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCn1cc[n+](CC(O)CO)c1.[Cl-]
Reaction #90826
product
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCn1cc[n+](CC(O)CO)c1.[Cl-]
Reaction #90827
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCn1cc[n+](CC(O)CO)c1.[Cl-]
Reaction #90828
product
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
OCC(O)C[n+]1ccn(Cc2ccccc2)c1.[Cl-]
Reaction #90829
product
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
OCC(O)Cn1ccnc1
Reaction #90830
solid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[N+](C)(C)CC(O)CO
Reaction #183876
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccc(C2(c3ccc(F)cc3)OCC(CCl)O2)cc1
Reaction #185191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCn1c(=O)c2c(ncn2CC(O)CO)n(CCC)c1=O
Reaction #188406
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(CNC(=O)c2sc(C)c3c2CC2C3C2(C)C)cc(C)c1OCC(O)CO
Reaction #197283
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(-c2ncc(-c3cc(C)nc(NC(C)C)n3)o2)cc(C)c1OCC(O)CO
Reaction #229169
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(=C(c1ccccc1)c1ccc(OCC(O)CO)cc1)C1CCCC1
Reaction #262157
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1Nc2ccc(OCC(O)CO)cc2C1=Cc1c[nH]c2ncccc12
Reaction #275123
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1ccc(-c2nc(-c3cc(C)c(OCC(O)CO)c(C)c3)no2)s1
Reaction #278088
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)CC1(C)OCC(CCl)O1
Reaction #282861
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCC(O)CSc1nc2ccccc2s1
Reaction #291238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1=CCCCC(=O)OCCCCCCCCC1
Reaction #292662
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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