Furtrethonium iodide

Base Information

• Chemical Name: Furtrethonium iodide
• CAS No.: 541-64-0
• Molecular Formula: C8H14 N O . I
• Molecular Weight: 267.11
• Hs Code.: 2932190090
• European Community (EC) Number: 208-789-5
• NSC Number: 27126
• UNII: 1D064NLD7G
• DSSTox Substance ID: DTXSID60968970
• Wikidata: Q27252252
• NCI Thesaurus Code: C76041
• ChEMBL ID: CHEMBL2105806
• Mol file: 541-64-0.mol

Synonyms:furfuryltrimethylammonium;Furmethide;furtrethonium;furtrethonium benzenesulfonate;furtrethonium besylate;furtrethonium bromide;furtrethonium chloride;furtrethonium hydroxide;furtrethonium iodide

Chemical Property of Furtrethonium iodide

Chemical Property:

• Melting Point: 116-117° (Weilmuenster, Jordan); mp 118-120° (Khromov-Borisov)
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 13.14000
• Density: g/cm³
• LogP: -1.51020
• Storage Temp.: -196°C
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 267.01201
• Heavy Atom Count: 11
• Complexity: 106

Purity/Quality:

98%min ^*data from raw suppliers

FURMETHIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[N+](C)(C)CC1=CC=CO1.[I-]
• Therapeutic Function: Cholinergic

Technology Process of Furtrethonium iodide

There total 3 articles about Furtrethonium iodide 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:

furan-2-ylmethanamine (617-89-0) + methyl iodide (74-88-4) → Furmethide (541-64-0)

Guidance literature:

With methanol; man zersetzt durch feuchtes Silberoxyd;

Reference yield:

→ Furmethide (541-64-0)

Guidance literature:

With methyl iodide;

DOI:10.1021/ja01219a019

Reference yield:

furan-2-ylmethanamine (617-89-0) → Furmethide (541-64-0)

Guidance literature:

With potassium carbonate; methyl iodide;

upstream raw materials:

furan-2-ylmethanamine

methyl iodide

Downstream raw materials:

furfurylacetate

2-[(phenylsulfonyl)methyl]furan

5-methyl-furan-2-carbonitrile

(furan-2-ylmethyl)dimethylamine

Refernces