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4,7-Bis(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-2,1,3-Benzothiadiazole CAS NO 934365-16-9


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CAS No.:934365-16-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

4,7-Bis(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-2,1,3-Benzothiadiazole is a high-purity, functionalized benzothiadiazole derivative featuring two pinacol boronate ester groups, making it a critical advanced intermediate for cross-coupling reactions. This compound matters for its role as a key building block in the synthesis of complex organic electronic materials, enabling precise molecular engineering. It is primarily needed by R&D chemists and process engineers in the organic electronics, pharmaceutical, and agrochemical industries for constructing conjugated polymers, small molecule semiconductors, and other functional materials.

Application

  • Suzuki-Miyaura Cross-Coupling Reactions: As a versatile bis-boronic ester monomer for constructing conjugated polymers and small molecules used in Organic Light-Emitting Diodes (OLEDs) and Organic Photovoltaics (OPVs).
  • Organic Semiconductor Synthesis: A key precursor for developing electron-accepting or ambipolar materials in field-effect transistors (OFETs) and other electronic devices.
  • Pharmaceutical Intermediate: Used in the research and development of novel drug candidates, particularly those requiring complex, conjugated heterocyclic cores.
  • Agrochemical Active Ingredient Development: Serves as a building block for creating new molecules with potential biological activity.
  • Material Science Research: For the development of novel dyes, sensors, and non-linear optical materials due to its electron-deficient benzothiadiazole core.
  • Ligand and Catalyst Design: Can be incorporated into frameworks for creating novel ligands or metal-organic frameworks (MOFs).

Basic Information

Product Name 4,7-Bis(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-2,1,3-Benzothiadiazole
CAS No. 934365-16-9
Molecular Formula C22H32B2N2O4S
Molecular Weight 442.10 g/mol
Synonyms 2,1,3-Benzothiadiazole-4,7-diyldiboronic acid bis(pinacol) ester; 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole; 4,7-Bis(pinacolatoboryl)-2,1,3-benzothiadiazole; 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[1,2,5]thiadiazole; 4,7-Di(1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole pinacol ester; BT-BPin; BBT-2BPin; 4,7-BisBPin-BT
EINECS Contact for details

Quality Control

Our 4,7-Bis(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-2,1,3-Benzothiadiazole is manufactured under strict quality control protocols to ensure batch-to-batch consistency and high purity for sensitive synthetic applications. We provide comprehensive Certificates of Analysis (COA) with each batch, detailing key parameters such as purity (HPLC/NMR), identity, and impurity profiles. Our quality system is designed to meet the stringent requirements of research and process development in advanced material science.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and should be handled under an inert atmosphere (e.g., nitrogen or argon) for long-term storage and when dispensing to prevent hydrolysis of the boronate ester groups. Keep container tightly sealed when not in use.

Specification

Item Specification
Appearance Yellow to orange crystalline powder
Identification (IR) Conforms to structure
Purity (HPLC) ≥ 97.0% (Area %)
Purity (NMR) ≥ 95.0%
Melting Point Contact for details
Heavy Metals < 20 ppm
Residual Solvents (GC) Meets ICH guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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