1369328-62-0

Basic information

• Product Name: 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid
• Synonyms: 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid;5'-Formyl-2,2'-bithiophene-5-boronic Acid (contains varying amounts of Anhydride)
• CAS NO: 1369328-62-0
• Molecular Formula: C₉H₇BO₃S₂
• Molecular Weight: 238.09108
• EINECS: 811-036-9
• Product Categories: B (Classes of Boron Compounds);Boronic Acids;Functional Materials;Reagents for Conducting Polymer Research;Thiophene Derivatives (for Conduting Polymer Research)
• Mol File: 1369328-62-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 0-10°C
• CAS DataBase Reference: 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid(1369328-62-0)
• EPA Substance Registry System: 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid(1369328-62-0)

Safety Data

• Hazardous Substances Data: 1369328-62-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid is used as a building block in organic synthesis for constructing complex molecules. Its boronic acid functionality allows it to form stable complexes with diols, facilitating the synthesis of a wide range of chemical structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid is used as a key intermediate in the development of pharmaceuticals. Its unique structure and reactivity enable the creation of novel compounds with potential therapeutic properties.
Used in Agrochemical Development:
5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid is also utilized in the development of agrochemicals, where its chemical properties can be harnessed to create new compounds with pesticidal or herbicidal activities.
Used in the Synthesis of Biologically Active Compounds:
Due to its potential biological activities, 5-(5-Formyl-2-thienyl)-2-thiopheneboronic Acid is used as a starting material in the synthesis of biologically active compounds. Its formyl group and thiophene ring can be further modified to generate a variety of molecules with potential applications in drug discovery and development.

Upstream product

• 492-97-7 2,2'-Bithiophene 
• 773093-00-8 2-(5’-bromo-[2,2’-bithiophen]-5-yl)-1,3-dioxolane 
• 110046-60-1 5'-bromo-2,2'-bithiophene-5-carboxaldehyde 
• 3779-27-9 2,2'-bithiophene-5-carboxaldehyde 

Downstream Products

• 1440528-95-9 5’-(4-(bis(1,3-dihexyl-2-thioxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)amino)phenyl)-[2,2’-bithiophene]-5-carbaldehyde 
• 1440530-46-0 (E)-3-(5’-(4-(bis(1,3-dihexyl-2-thioxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)amino)phenyl)-[2,2’-bithiophen]-5-yl)-2-cyanoacrylic acid 
• 1219091-31-2 5′-(4-(bis(4-methoxyphenyl)amino)phenyl)-[2,2′-bithiophene]-5-carbaldehyde 

Relevant articles and documents

Cyclic thiourea/urea functionalized triphenylamine-based dyes for high-performance dye-sensitized solar cells

Six cyclic thiourea/urea functionalized triphenylamine-based dyes (AZ1-AZ6) containing 2-cyanoacrylic acid as an acceptor and various linkers (phenyl, biphenyl, and bithiophene) were synthesized. They exhibited high photovoltaic performance owing to an improved short-circuit photocurrent density (J sc) and open-circuit voltage (Voc). Among them, AZ6 bearing a cyclic thiourea group and bithiophene linker showed the highest power conversion efficiency (PCE) up to 7.29%, which was comparable to that of N719 (PCE = 7.36%).