مشارك في 260 تفاعل

C(C(=O)N)Cl

COC(=O)NC(=O)CCl
Reaction #55689
methyl(chloroacetyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
NC(=O)CON=C(c1ccc(Cl)cc1)c1ccc(Cl)cc1
Reaction #75359
di-(4-chlorophenyl)methyleneamino-oxyacetamide
المردود 35.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCOC(=O)CCNCC(N)=O
Reaction #79462
title compound
المردود 51.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
NC(=O)Cn1c(-c2ccc(Cl)cc2)nc2ncccc21
Reaction #193024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)CN1CCc2ccc(OCc3cccc(F)c3)cc2CC1
Reaction #201513
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc2nc(Cn3cnc4c(N)ncnc43)n(-c3ccccc3OCC(N)=O)c(=O)c12
Reaction #208781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(Cc1cnc2cc(OCC(N)=O)ccn12)[N+](=O)[O-]
Reaction #210655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc2cccc(OCC(N)=O)c2n1C
Reaction #224118
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)CON1C(=O)c2ccccc2C1=O
Reaction #232829
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)CN(CCc1cccc(OCc2cccc(F)c2)c1)Cc1ccco1
Reaction #243260
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)COC(=O)Cc1ccc(O)cc1
Reaction #244209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)CON=C(c1ccc(Cl)cc1)c1ccc(Cl)cc1
Reaction #250688
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)CSC(c1ccccc1)c1ccccc1
Reaction #258148
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1c(-c2ccccc2)c2cc(Cl)ccc2n1CC(N)=O
Reaction #280920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)CN1CCC(C(=O)N2CCN3C(=O)OC(c4ccccc4)(c4ccccc4)C3C2)CC1
Reaction #282302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)N1CCC2(CCN(CC(N)=O)CC2)CC1
Reaction #290574
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)CNc1ccccc1
Reaction #292229
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)N1CCN(c2nc(C)nc3c2OCC(=O)N3CC(N)=O)CC1
Reaction #294375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)C[n+]1ccccc1.[Cl-]
Reaction #331786
1-(2-amino-2-oxoethyl)pyridinium chloride
المردود 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCCCC(C)C(C)c1cc(O)c2c(c1)OC(C)(C)C1=C2CN(CC(N)=O)CC1
Reaction #348913
10-Hydroxy-5,5-dimethyl-8-(1,2-dimethylheptyl)-1,2,3,4-tetrahydro-5H-[1]benzopyrano[4,3-c]pyridine-2-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
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