dimethylthiocarbamoyl chloride

CN(C)C(=S)Oc1cccc(C#N)c1
Reaction #6097
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)C(=S)Oc1ccccc1C#N
Reaction #6100
expected product
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)C(=S)Oc1ccccc1C(F)(F)F
Reaction #6109
yellow oil
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(Br)ccc1OC(=S)N(C)C
Reaction #41507
O-4-bromo-2-methoxyphenyl dimethylcarbamothioate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(OC(=S)N(C)C)c(C(C)(C)C)cc1C=O
Reaction #51745
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)c1ccc(OC(=S)N(C)C)c(C(C)(C)C)c1
Reaction #51746
3-tert-butyl-4-dimethylthiocarbamoyloxy-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)C(=S)Oc1ccc2c(c1)C(=O)CCC2(C)C
Reaction #81553
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CN(C)C(=S)Oc1ccc(Br)cc1C=O
Reaction #82230
5-bromo-2-[(N,N-dimethylthiocarbamoyl)oxy]benzaldehyde
المردود 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cc(OC(=S)N(C)C)nc(C(Cl)(Cl)Cl)n1
Reaction #94997
product
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COC(C(=S)N(C)C)c1ccccn1
Reaction #173872
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C(=S)Oc1ccc(C(=O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #194934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(F)ccc1OC(=S)N(C)C
Reaction #198391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCOC(=O)c1ncc2cc(Oc3ccccc3)ccc2c1OC(=S)N(C)C
Reaction #200890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C(=S)Oc1cc(CC(=O)O)cc(C(F)(F)F)c1
Reaction #212128
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(OC(=S)N(C)C)c(C23CC4CC(CC(C4)C2)C3)c1
Reaction #216859
expected product
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CN(C)C(=S)Oc1cc2c(cc1C#N)CCCC2
Reaction #218360
dimethyl-thiocarbamic acid O-(3-cyano-5,6,7,8-tetrahydro-naphthalene-2-yl) ester
المردود 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CN(C)C(=S)Oc1ccc(S(=O)(=O)c2ccc(C#N)cc2)cc1
Reaction #223228
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cccc(C=O)c1OC(=S)N(C)C
Reaction #238908
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(OC(=S)N(C)C)nc(C(Cl)(Cl)Cl)n1
Reaction #243678
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C)C(=S)n1cnc(S(=O)(=O)CC2CCCC2)n1
Reaction #252035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
الصفحة 1التالي