N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate

Base Information

Chemical Name:N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate
CAS No.:85894-20-8
Molecular Formula:C₇H₈O₃S*C₈H₉IN₄O
Molecular Weight:476.295
Hs Code.:
NSC Number:355190

Synonyms:NSC 355190;N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate;85894-20-8;Hydrazinecarboximidamide, N-hydroxy-2-((3-iodophenyl)methylene)-, mono(4- methylbenzenesulfonate) (salt);NSC355190;C8H9IN4O.C7H8O3S;NSC-355190;LS-76653;C8-H9-I-N4-O.C7-H8-O3-S

Suppliers and Price of N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate

Chemical Property:

Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:476.00152
Heavy Atom Count:25
Complexity:438

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)O.C1=CC(=CC(=C1)I)C=NN=C(N)NO
Isomeric SMILES:CC1=CC=C(C=C1)S(=O)(=O)O.C1=CC(=CC(=C1)I)/C=N/N=C(\N)/NO

Technology Process of N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate

There total 4 articles about N-Hydroxy-2-((3-iodophenyl)methylene)hydrazinecarboximidamide tosylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.96%

: 696-41-3
m-iodobenzaldehyde

: 36826-58-1
N-hydroxy-N'-aminoguanidine p-toluenesulphonate

: 85894-20-8
1-<(3iodobenzylidene)amino>-3-hydroxyguanidine tosylate

Guidance literature:: DOI:10.1021/jm00368a024

Reference yield:

: 36778-68-4
S-methylisothiosemicarbazide tosylate

: 85894-20-8
1-<(3iodobenzylidene)amino>-3-hydroxyguanidine tosylate

Guidance literature:: Multi-step reaction with 2 steps

1: 44.2 percent / hydroxylamine / 48 h / Ambient temperature

2: 88.96 percent

With hydroxylamine;
DOI:10.1021/jm00368a024

Reference yield:

: 80-48-8
methyl p-toluene sulfonate

: 85894-20-8
1-<(3iodobenzylidene)amino>-3-hydroxyguanidine tosylate

Guidance literature:: Multi-step reaction with 3 steps

1: 135 g / CH₃OH / 18 h / Heating

2: 44.2 percent / hydroxylamine / 48 h / Ambient temperature

3: 88.96 percent

With methanol; hydroxylamine;
DOI:10.1021/jm00368a024