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Available Variants1 g
CHA.51288-1g
Price
€128.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.51288-1g | €128.80 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C9H9BO2 |
|---|---|
| CAS Number | 312968-21-1 |
| Molecular Weight | 159.98 |
| NACRES | NA.22 |
| PubChem Substance ID | 329766997 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD11506071 |
| Form | solid |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
1H-Indene-2-boronic acid, with the CAS registry number 312968-21-1, is a boronic acid derivative of indene, exhibiting unique chemical properties. This compound is utilized as a building block in various organic synthesis reactions, particularly in the formation of complex molecules through cross-coupling reactions. The presence of the boronic acid functional group enables it to participate in Suzuki-Miyaura coupling reactions, allowing for the creation of carbon-carbon bonds with aryl halides. As a result, 1H-Indene-2-boronic acid has become a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its reactivity and versatility make it a sought-after compound in modern organic chemistry, facilitating the development of novel compounds with potential biological and technological significance.
