methyl carbamimidothioate

Reaction #40535
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N=C(N)NCCCSc1ncco1
Reaction #55829
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
N=C(N)NCCSCc1ccon1
Reaction #55833
[2-(3-isoxazolylmethylthio)ethyl]guanidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
N=C(N)NCCCCN
Reaction #63026
4-guanidino-1-butanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
N=C(N)NCCCCCCN
Reaction #63029
6-guanidino-1-hexanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCOC(=O)c1cnc(SC)nc1C
Reaction #69756
solid
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CSC(=N)NC(=O)OCc1ccccc1
Reaction #95984
Benzyloxycarbonyl-S-methyl-isothiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CSc1nccc(C(=O)O)n1
Reaction #155472
2-(methylthio)pyrimidine-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N=C(N)Nc1cc(N)nc(NC(=N)N)n1
Reaction #181838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(N)NCC1(O)COc2ccccc2OC1
Reaction #201129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(N)N1CCc2[nH]cnc2C1
Reaction #213463
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(N)N1CCN(C23CC4CC(CC(C4)C2)C3)CC1
Reaction #235230
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSC(=N)NS(=O)(=O)CCl
Reaction #240828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc[nH]c1CSCCN=C(N)N
Reaction #250629
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N=C(N)NCC(CNS(=O)(=O)c1cccc2cnccc12)c1ccccc1
Reaction #256520
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN1CCN(C(=N)N)CC1
Reaction #277475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N=C(N)N1CCC(CCC(=O)O)CC1
Reaction #281762
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N=C(N)NCCCSc1ncco1
Reaction #349847
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
N=C(N)NCCSCc1ccon1
Reaction #349851
[2-(3-isoxazolylmethylthio)ethyl]guanidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
N=C(N)NCCNS(=O)(=O)c1cccc2cnccc12
Reaction #369108
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
الصفحة 1التالي