1H-Indene-2-boronic acid pinacol ester
1H-Indene-2-boronic acid pinacol ester (CAS 749869-98-5, C15H19BO2) is an organoboron compound with a molecular weight of 242.12 g/mol. This compound serves as a valuable building block in organic synthesis, particularly in cross-coupling reactions. Its structure, featuring an indene core attached to a boronate ester moiety, makes it a versatile reagent for the introduction of the indene group into various molecular architectures.
- IUPAC
- 2-(1H-Inden-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- Synonyms
- 2-(1H-Inden-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Suzuki-Miyaura Coupling Reactions
This pinacol ester is widely employed as a coupling partner in Suzuki-Miyaura reactions. It facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules containing the indene framework.
Organic Synthesis Intermediate
As a functionalised indene derivative, it is a key intermediate in the multi-step synthesis of diverse chemical entities. Its reactivity allows for further functionalization and elaboration into more complex structures for research and development.
Materials Science Research
The indene moiety can be incorporated into conjugated systems, making this boronate ester a potential precursor for materials with interesting electronic or optical properties in materials science research.
| Molecular weight | 242.12 |
|---|---|
| Empirical formula | C15H19BO2 |
| Assay | 97% |
| Storage temperature | 2-8°C |
| Melting point | 72-80 °C |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is 1H-Indene-2-boronic acid pinacol ester used for?
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1H-Indene-2-boronic acid pinacol ester is primarily used as a building block in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions to introduce the indene moiety into target molecules.
What are the CAS number and formula for 1H-Indene-2-boronic acid pinacol ester?
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The CAS number is 749869-98-5 and the empirical formula (Hill notation) is C15H19BO2.
What grade and purity does Tech Serve Solutions supply?
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Tech Serve Solutions supplies 1H-Indene-2-boronic acid pinacol ester with a purity of 97%. We do not represent this product as USP, BP, EP, or any other pharmacopoeial grade.
How should 1H-Indene-2-boronic acid pinacol ester be handled and stored?
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This compound has a GHS hazard classification of WGK 3. It should be stored at refrigeration temperatures between 2-8°C. Handle with appropriate personal protective equipment in a well-ventilated area.
Is 1H-Indene-2-boronic acid pinacol ester a controlled substance?
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The provided data does not indicate that 1H-Indene-2-boronic acid pinacol ester is a controlled substance.
How is 1H-Indene-2-boronic acid pinacol ester packed and shipped?
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Products are carefully packed according to international shipping regulations for hazardous materials and exported globally by Tech Serve Solutions.
How can I request a quote or sample of 1H-Indene-2-boronic acid pinacol ester?
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Please contact our sales team or use the online portal to request a quote or sample of 1H-Indene-2-boronic acid pinacol ester.
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