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2,3′-Bithiophene

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For Research Use Only | Not For Clinical Use
CATAP2404899
CAS2404-89-9
Structure
MDL NumberMFCD04039963
Molecular Weight166.26
InChI KeyILQGHVXNYGLZSR-UHFFFAOYSA-N
Description96%
Assay96%
MP60-64 °C (lit.)
Size1G
1

2,2',5,5'-tetramethyl-4,4'-bis(diphenylphoshino)-3,3'-bithiophene: A New, Very Efficient, Easily Accessible, Chiral Biheteroaromatic Ligand for Homogeneous Stereoselective Catalysis

T Benincori, E Cesarotti, O Piccolo, F Sannicolo

J Org Chem. 2000 Apr 7;65(7):2043-7.

PMID: 10774024

1

Highly Enantioselective "Inherently Chiral" Electroactive Materials Based on a 2,2'-biindole Atropisomeric Scaffold

Serena Arnaboldi, Tiziana Benincori, Andrea Penoni, Luca Vaghi, Roberto Cirilli, Sergio Abbate, Giovanna Longhi, Giuseppe Mazzeo, Sara Grecchi, Monica Panigati, Patrizia Romana Mussini

Chem Sci. 2019 Jan 5;10(9):2708-2717.

PMID: 30996988

1

Large-scale High-Throughput Screening Revealed 5'-(carbonylamino)-2,3'-bithiophene-4'-carboxylate as Novel Template for Antibacterial Agents

Yan A Ivanenkov, Renat S Yamidanov, Ilya A Osterman, Petr V Sergiev, Vladimir A Aladinskiy, Anastasia V Aladinskaya, Victor A Terentiev, Mark S Veselov, Andrey A Ayginin, Dmitry A Skvortsov, Katerina S Komarova, etc.

Curr Drug Discov Technol. 2019 Jun 2.

PMID: 31161993

1

Ring-opening Reaction of 2,5-dioctyldithieno[2,3-b:3',2'-d]thiophene in the Presence of Aryllithium Reagents

Hao Zhong, Jianwu Shi, Jianxun Kang, Shaomin Wang, Xinming Liu, Hua Wang

Beilstein J Org Chem. 2013 Apr 19;9:767-74.

PMID: 23766789

1

Synthesis and Molecular Docking of New Thiophene Derivatives as Lactate Dehydrogenase-A Inhibitors

Abd El-Galil E Amr, Mohamed F El-Shehry, Alhussein A Ibrahim, Hanaa M Hosni, Mohamed A Al-Omar, Hazem A Ghabbour

Mini Rev Med Chem. 2019;19(10):833-841.

PMID: 30760188

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