Methfuroxam

Base Information

• Chemical Name: Methfuroxam
• CAS No.: 28730-17-8
• Molecular Formula: C14H15 N O2
• Molecular Weight: 229.279
• Hs Code.: 2932190012
• European Community (EC) Number: 249-194-0
• UNII: 4K9VG91RQZ
• DSSTox Substance ID: DTXSID8042137
• Nikkaji Number: J21.655K
• Wikidata: Q22808392
• ChEMBL ID: CHEMBL1395509
• Mol file: 28730-17-8.mol

Synonyms:2,4,5-trimethyl-N-phenyl-3-furancarboxamide;3-furanilide, 2,4,5-trimethyl-;methfuroxam;methfuroxan

Chemical Property of Methfuroxam

Chemical Property:

• Vapor Pressure: 0.00101mmHg at 25°C
• Boiling Point: 302.2oC at 760 mmHg
• Flash Point: 136.6oC
• PSA: 42.24000
• Density: 1.146g/cm3
• LogP: 3.53010
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 229.110278721
• Heavy Atom Count: 17
• Complexity: 273

Purity/Quality:

98%Min ^*data from raw suppliers

Methfuroxam ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 22

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=C(OC(=C1C(=O)NC2=CC=CC=C2)C)C
• Recent EU Clinical Trials: First line standard therapy of glioblastoma multiforme with or without add-on treatment with Trivax, an anti-tumour immune therapy based on tumour-lysate charged dendritic cells
• Uses: Methfuroxam is an analytical standard used for biochemical research.

Technology Process of Methfuroxam

There total 1 articles about Methfuroxam 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:

→ 2,4,5-trimethyl-furan-3-carboxanilide (28730-17-8)

Guidance literature:

Reference yield:

2,4,5-trimethyl-furan-3-carboxanilide (28730-17-8) → 1,3,5-Trimethyl-2,6-dioxa-bicyclo[3.1.0]hex-3-ene-4-carboxylic acid phenylamide

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In [D₃]acetonitrile; at 0 ℃;

DOI:10.1039/c39850001642

Reference yield:

2,4,5-trimethyl-furan-3-carboxanilide (28730-17-8) → (E)-2-Acetyl-3-methyl-4-oxo-pent-2-enoic acid phenylamide

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In [D₃]acetonitrile; at 25 ℃; Yield given;

DOI:10.1039/c39850001642

Downstream raw materials:

N-(fluorodichloromethylthio-)2,4,5-trimethyl-furan-3-carboxanilide

Refernces

• 1、 -. "Organosilyl compounds and their use as fungicides". . . Retrieved 2008/06/13.