[4-(Thiophene-2-carbonyl)-phenyl]-thiophen-2-YL-methanone

Base Information

• Chemical Name: [4-(Thiophene-2-carbonyl)-phenyl]-thiophen-2-YL-methanone
• CAS No.: 148982-08-5
• Molecular Formula: C16H10 O2 S2
• Molecular Weight: 298.38
• DSSTox Substance ID: DTXSID10364084
• Wikidata: Q82147847
• Mol file: 148982-08-5.mol

Synonyms:148982-08-5;[4-(THIOPHENE-2-CARBONYL)-PHENYL]-THIOPHEN-2-YL-METHANONE;[4-(thiophene-2-carbonyl)phenyl]-thiophen-2-ylmethanone;1,4-di(2-thenoyl)benzene;SCHEMBL6793430;DTXSID10364084;(1,4-Phenylene)bis[(thiophen-2-yl)methanone];[4-(thiophene-2-carbonyl)phenyl]thiophen-2-ylmethanone

Chemical Property of [4-(Thiophene-2-carbonyl)-phenyl]-thiophen-2-YL-methanone

Chemical Property:

• PSA: 90.62000
• LogP: 4.27160
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 298.01222190
• Heavy Atom Count: 20
• Complexity: 339

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CSC(=C1)C(=O)C2=CC=C(C=C2)C(=O)C3=CC=CS3

Technology Process of [4-(Thiophene-2-carbonyl)-phenyl]-thiophen-2-YL-methanone

There total 2 articles about [4-(Thiophene-2-carbonyl)-phenyl]-thiophen-2-YL-methanone 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: 65.0%

thiophene (188290-36-0,8014-23-1,25233-34-5) + terephthaloyl chloride (100-20-9) → 1,4-phenylene bis(2-thienylmethanone) (148982-08-5)

Guidance literature:

With aluminium trichloride; In dichloromethane; for 4h; Ambient temperature;

Reference yield:

thiophene boronic acid (6165-68-0) + terephthaloyl chloride (100-20-9) → 1,4-phenylene bis(2-thienylmethanone) (148982-08-5)

Guidance literature:

With lithium hydroxide monohydrate; PdCl2{κ²?N,S?2?(4,5-dihydrothiazol-2-yl)aniline}; In acetonitrile; at 80 ℃; for 0.333333h; Catalytic behavior;

DOI:10.1016/j.ica.2018.09.012

Reference yield: 86.0%

C5H8O3PS2(1-)*Li(1+) + 1,4-phenylene bis(2-thienylmethanone) (148982-08-5) → 1,4-Bis<1-(1,3-dithiol-2-ylidene)-2-thienylmethyl>benzene

Guidance literature:

In tetrahydrofuran; 1.) -78 deg C, 1 h, 2.) RT, 6.5 h;

DOI:10.1039/c39930000431

upstream raw materials:

thiophene

terephthaloyl chloride

thiophene boronic acid

Downstream raw materials:

1-{4-[1-(2-thienyl)-2,2-diphenylvinyl]phenyl}-1-(2-thienyl)-2,2-diphenylethene