Aminoguanidine bicarbonate

Nc1nnc(-c2cc(Cl)cc(Cl)c2Cl)c(N)n1
Reaction #833094
3,5-diamino-6-(2,3,5-trichlorophenyl)-1,2,4 -triazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
Cl.N=C(N)NN=Cc1c(Cl)ccc([N+](=O)[O-])c1Cl
Reaction #833218
(2,6-dichloro-3-nitrobenzylideneamino)-guanidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
Cl.N=C(N)NN=Cc1c(Cl)cc([N+](=O)[O-])cc1Cl
Reaction #833223
(2,6-dichloro-4-nitrobenzylidene amino)-guanidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
Nc1nc(COC(=O)CO)n[nH]1
Reaction #945916
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_12
CC(C)(F)c1cnnc(N)n1
Reaction #979034
title compound
Rendimiento 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
Nc1nncc(C(F)(F)F)n1
Reaction #979039
mixture
Rendimiento 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
NC(N)=[NH2+].NC(N)=[NH2+].O=C([O-])C(=O)[O-]
Reaction #992675
Guanidinium Oxalate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
NC(N)=[NH2+].NC(N)=[NH2+].O=C([O-])CC(=O)[O-]
Reaction #992676
Guanidinium Malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
NNC(N)=[NH2+].NNC(N)=[NH2+].O=C([O-])C(=O)[O-]
Reaction #992689
Bis(aminoguanidinium) Oxalate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
NNC(N)=[NH2+].NNC(N)=[NH2+].O=C([O-])[C@H](O)[C@@H](O)C(=O)[O-]
Reaction #992692
Bis(aminoguanidinium) L-Tartrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
NNC(N)=[NH2+].NNC(N)=[NH2+].O=C([O-])CC(O)C(=O)[O-]
Reaction #992693
Bis(aminoguanidinium) DL-Malate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
NNC(N)=[NH2+].NNC(N)=[NH2+].NNC(N)=[NH2+].O=C([O-])CN(CC(=O)[O-])CC(=O)[O-]
Reaction #992695
Tris(aminoguanidinium) Nitrilotriacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
NNC(N)=[NH2+].O=C/C(Br)=C(/Br)C(=O)[O-]
Reaction #992696
Aminoguanidinium Mucobromate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CCOC(=O)C(=O)NNC(=N)N
Reaction #1010500
ethyl 2-(2-carbamimidoylhydraziny)-2-oxoacetic acid
Rendimiento 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
N=C(N)NNC(=O)c1ccc(Cl)c(Cl)c1
Reaction #1010508
2-(3,4-dichlorobenzoyl)hydrazinecarboximidamide
Rendimiento 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
N=C(N)NNC(=O)c1cccc(Cl)c1
Reaction #1010513
2-(3-chlorobenzoyl)hydrazinecarboximidamide
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC(C)c1n[nH]c(N)n1
Reaction #1010517
3-isopropyl-1H-1,2,4-triazol-5-amine
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
N=C(N)NNC(=O)c1ccc(Cl)cc1
Reaction #1010520
2-(4-chlorobenzoyl)hydrazinecarboximidamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
N=C(N)NNC(=O)c1ccccc1Cl
Reaction #1010531
2-(2-Chlorobenzoyl)hydrazinecarboximidamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cc1ccccc1C(=O)NNC(=N)N
Reaction #1010535
2-(2-methylbenzoyl)hydrazinecarboximidamide
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
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