Methyl furan-2-carboximidate

Base Information

• Chemical Name: Methyl furan-2-carboximidate
• CAS No.: 51282-48-5
• Molecular Formula: C6H7NO2
• Molecular Weight: 125.127
• Hs Code.: 2932190090
• DSSTox Substance ID: DTXSID60519087
• Wikidata: Q82382033
• Mol file: 51282-48-5.mol

Synonyms:Methyl furan-2-carbimidate;51282-48-5;Methyl furan-2-carboximidate;2-Furancarboximidic acid, methyl ester;Methylfuran-2-carbimidate;methyl 2-furancarboximidate;SCHEMBL9216297;DTXSID60519087;LXAAUEZVEFPTPX-UHFFFAOYSA-N;BCA28248;AKOS010211876;A918342

Chemical Property of Methyl furan-2-carboximidate

Chemical Property:

• PSA: 46.22000
• LogP: 1.35110
• Storage Temp.: 2-8°C
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 125.047678466
• Heavy Atom Count: 9
• Complexity: 114

Purity/Quality:

97% ^*data from raw suppliers

Methylfuran-2-carbimidate 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC(=N)C1=CC=CO1

Technology Process of Methyl furan-2-carboximidate

There total 1 articles about Methyl furan-2-carboximidate 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:

furfural (98-01-1) + methanol (67-56-1) → 2-furancarbonitrile (617-90-3) + furane-2-carboximidate de methyle (51282-48-5)

Guidance literature:

With ammonia; oxygen; In water; at 30 ℃; for 12h; under 3750.38 Torr; Mechanism; Autoclave;

DOI:10.1039/c6cy00874g

Reference yield: 78.0%

furane-2-carboximidate de methyle (51282-48-5) + 1-((dimethylamino)(phenyl)methyl)naphthalen-2-ol (39487-54-2) → 3-(furan-2-yl)-1-phenyl-1H-naphtho[1,2-e][1,3]oxazine

Guidance literature:

In N,N-dimethyl-formamide; for 6h; Reflux;

DOI:10.1021/acs.joc.8b00692

Reference yield: 65.0%

furane-2-carboximidate de methyle (51282-48-5) + 1-[(dimethylamino)(2-methoxyphenyl)methyl]naphthalen-2-ol → 3-(furan-2-yl)-1-(2-methoxyphenyl)-1H-naphtho[1,2-e][1,3]oxazine

Guidance literature:

In N,N-dimethyl-formamide; for 8h; Reflux;

DOI:10.1021/acs.joc.8b00692

upstream raw materials:

furfural

methanol

Downstream raw materials:

5-(2-amino-4-chlorophenyl)-3-(2-furyl)-1H-1,2,4-triazole

4-Chloro-2-<3-(2-furanyl)-1H-1,2,4-triazol-5-yl>benzeneamine

9-chloro-2-(2-furanyl)-[1,2,4]triazolo[1,5-C]quinazolin-5-amine

5-(2-aminophenyl)-3-(2-furyl)-1H-1,2,4-triazole

Refernces