Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride

Base Information

Chemical Name:Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride
CAS No.:75745-70-9
Molecular Formula:C₁₃H₁₃N₃O₄S*ClH
Molecular Weight:343.791
Hs Code.:
DSSTox Substance ID:DTXSID70226634
Mol file:75745-70-9.mol

Synonyms:75745-70-9;Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride;N-(4-((5-(Aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)acetamide monohydrochloride;C13H13N3O4S.ClH;DTXSID70226634;C13-H13-N3-O4-S.Cl-H;LS-8054;Acetamide,N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-,monohydrochloride

Suppliers and Price of Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride

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 4 raw suppliers

Chemical Property of Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride

Chemical Property:

Vapor Pressure:1.9E-15mmHg at 25°C
Boiling Point:616.2°C at 760 mmHg
Flash Point:326.5°C
PSA：138.12000
LogP:4.68720
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:343.0393548
Heavy Atom Count:22
Complexity:506

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(O2)C(=N)N.Cl

Technology Process of Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride

There total 3 articles about Acetamide, N-(4-((5-(aminoiminomethyl)-2-furanyl)sulfonyl)phenyl)-, monohydrochloride 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: 78.0%

: 5-<(4-acetamidophenyl)sulphonyl>-2-furancarboximidate HCl

: 75745-70-9
5-<(4-acetamidophenyl)sulphonyl>-2-furancarboxamidine HCl

Guidance literature:: With ammonia; for 48h; Ambient temperature;

Reference yield:

: 61942-48-1
5-<(4-acetamidophenyl)sulphonyl>-2-furancarboxaldehyde

: 75745-70-9
5-<(4-acetamidophenyl)sulphonyl>-2-furancarboxamidine HCl

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / NH₂OH*HCl, Ac₂O / methanol / 1 h / Heating

2: HCl(g) / 48 h / 0 - 5 °C

3: 78 percent / 28percent NH₃ (methanolic) / 48 h / Ambient temperature

With hydrogenchloride; hydroxylamine hydrochloride; ammonia; acetic anhydride; In methanol;

Reference yield:

: 75745-65-2
5-<(4-acetamidophenyl)sulphonyl>-2-furancarbonitrile

: 75745-70-9
5-<(4-acetamidophenyl)sulphonyl>-2-furancarboxamidine HCl

Guidance literature:: Multi-step reaction with 2 steps

1: HCl(g) / 48 h / 0 - 5 °C

2: 78 percent / 28percent NH₃ (methanolic) / 48 h / Ambient temperature

With hydrogenchloride; ammonia;