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C(#N)N

CCN(CCCOC)C(=N)N
Reaction #859
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCNC(=N)N
Reaction #860
title compound
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCOCCOC(=O)c1ccccc1
Reaction #861
title compound
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1cccc(C(F)(F)F)c1.O=[N+]([O-])O
Reaction #2251
3-trifluoromethyl-phenylguanidine nitrate
DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=O)c1ccccc1
Reaction #4586
2
Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=O)C12CC3CC(CC(C3)C1)C2
Reaction #4587
4
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)NC#N
Reaction #4588
6
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)NC#N
Reaction #4589
Stearoylcyanamide
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=O)CNC(=O)c1ccccc1
Reaction #4590
N-Benzoylglycylcyanamide
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)c1ccccc1)C(=O)NC#N
Reaction #4592
N-Benzoyl-L-leucylcyanamide
Ausbeute 42.9%DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1
Reaction #4594
15
Ausbeute 42.5%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1cccc(OCc2ccccc2)c1
Reaction #6949
N-(3-Benzyloxy-phenyl)guanidine
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
NC(=[NH2+])Nc1ccccc1.O=[N+]([O-])[O-]
Reaction #8589
N-phenylguanidinium nitrate
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(N)=[NH2+])cc(OC)c1OC.O=[N+]([O-])[O-]
Reaction #8591
N-(3,4,5-trimethoxyphenyl)guanidinium nitrate
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(N)=[NH2+])cc1.O=[N+]([O-])[O-]
Reaction #8592
N-(4Methoxyphenyl)guanidinium nitrate
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=[NH2+])Nc1cccc(C(=O)c2ccccc2)c1.O=[N+]([O-])[O-]
Reaction #8598
N-(3-benzoylphenyl)guanidinium nitrate
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3nc(N)c(C(=O)c4ccc(Cl)c([N+](=O)[O-])c4)s3)cc2)CC1
Reaction #10894
[4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](4-chloro-3-nitrophenyl)methanone
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3nc(N)c(C(=O)c4ccc5c(c4)OCCO5)s3)cc2)CC1
Reaction #10895
[4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanone
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3nc(N)c(C(=O)c4ccc5c(c4)OCO5)s3)cc2)CC1
Reaction #10896
[4-Amino-2-[[4-(4-methyl-1-piperazi nyl)phenyl]amino]-5-thiazolyl](1,3-benzodioxol-5-yl)methanone
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3nc(N)c(C(=O)c4ccc(N5CCCC5)cc4)s3)cc2)CC1
Reaction #10897
[4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][4-(1-pyrrolidinyl) phenyl]methanone
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1
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