5-Phenylfuran-2-carbonyl chloride

Base Information

• Chemical Name: 5-Phenylfuran-2-carbonyl chloride
• CAS No.: 57489-93-7
• Molecular Formula: C11H7ClO2
• Molecular Weight: 206.628
• Hs Code.: 2932190090
• DSSTox Substance ID: DTXSID40378179
• Wikidata: Q82167707
• Mol file: 57489-93-7.mol

Synonyms:5-phenylfuran-2-carbonyl chloride;57489-93-7;5-Phenyl-2-furoyl chloride;5-PHENYL-FURAN-2-CARBONYL CHLORIDE;2-Furancarbonyl chloride, 5-phenyl-;5-PHENYL-FURAN-2-CARBONYLCHLORIDE;SCHEMBL221022;5-phenylfuran-2-carbonylchloride;DTXSID40378179;AKOS000296499;5-Phenyl-2-furoyl chloride, AldrichCPR;BB 0245437;FT-0767408

Chemical Property of 5-Phenylfuran-2-carbonyl chloride

Chemical Property:

• Vapor Pressure: 0.000183mmHg at 25°C
• Refractive Index: 1.564
• Boiling Point: 329°Cat760mmHg
• Flash Point: 152.8°C
• PSA: 30.21000
• Density: 1.26g/cm³
• LogP: 3.32560
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 206.0134572
• Heavy Atom Count: 14
• Complexity: 211

Purity/Quality:

99% ^*data from raw suppliers

5-PHENYLFURAN-2-CARBONYL CHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC=C(O2)C(=O)Cl

Technology Process of 5-Phenylfuran-2-carbonyl chloride

There total 8 articles about 5-Phenylfuran-2-carbonyl chloride 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: 100.0%

5-phenylfuran-2-carboxylic acid (52938-97-3) + oxalyl dichloride (79-37-8) → 5-phenyl-2-furancarbonyl chloride (57489-93-7)

Guidance literature:

In dichloromethane; N,N-dimethyl-formamide; at 25 ℃;

Reference yield:

aniline (62-53-3) → 5-phenyl-2-furancarbonyl chloride (57489-93-7)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride; sodium nitrite

2: thionyl chloride / benzene / 3 h / Reflux

With hydrogenchloride; thionyl chloride; sodium nitrite; In benzene; 1: Meerwein arylation;

DOI:10.1111/j.1747-0285.2011.01266.x

Reference yield:

2-furanoic acid (88-14-2) → 5-phenyl-2-furancarbonyl chloride (57489-93-7)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride; sodium nitrite

2: thionyl chloride / benzene / 3 h / Reflux

With hydrogenchloride; thionyl chloride; sodium nitrite; In benzene; 1: Meerwein arylation;

DOI:10.1111/j.1747-0285.2011.01266.x

upstream raw materials:

2-furanoic acid

aniline

5-phenylfuran-2-carboxylic acid

oxalyl dichloride

Downstream raw materials:

[(5-Phenyl-furan-2-carbonyl)-amino]-acetic acid ethyl ester

{[1-Chloro-1-(5-phenyl-furan-2-yl)-meth-(Z)-ylidene]-amino}-acetic acid ethyl ester

[5-(5-Phenyl-furan-2-yl)-tetrazol-1-yl]-acetic acid

ethyl 5-(5-phenyl-2-furyl)-1-tetrazolyl acetate

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