4-Isopropylbenzeneboronic acid, also called 4-isopropylphenylboronic acid, is an organoboron compound used mainly as a building block in organic synthesis. Its CAS Registry Number is 16152-51-5, its molecular formula is C9H13BO2, and its molar mass is approximately 164.01 g/mol. The molecule contains a phenyl ring bearing an isopropyl group and a boronic acid group in the para position. A common use is as an aryl coupling partner in Suzuki–Miyaura reactions, although suitability depends on the reaction design and the other reagents.
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This chemical is an aromatic boronic acid: a benzene ring is bonded to a boronic acid group, while an isopropyl substituent occupies the ring’s 4-position. The para arrangement distinguishes it from other positional isomers, such as ortho- or meta-substituted analogues. Its molecular formula, C9H13BO2, describes the atoms in one molecule, while the CAS number helps buyers and laboratories distinguish the substance in product records and purchasing systems.
The compound is generally considered a synthetic intermediate rather than a finished-use product. In research and process chemistry, chemists may evaluate it as a source of the 4-isopropylphenyl group when constructing more complex molecules. The exact application, reaction performance, and handling requirements depend on the intended synthesis and should be established through appropriate technical review.
| Property | Information |
|---|---|
| Product name | 4-Isopropylbenzeneboronic acid |
| Common systematic-style name | 4-Isopropylphenylboronic acid |
| CAS Number | 16152-51-5 |
| Molecular formula | C9H13BO2 |
| Molar mass | Approximately 164.01 g/mol |
| Functional class | Arylboronic acid |
The molar mass is useful for planning quantities, but it does not establish product purity or assay. For theoretical calculations, 1.00 mmol corresponds to approximately 164.0 mg of pure compound, and 10.00 mmol corresponds to approximately 1.640 g. Actual weighing and reaction charges should account for the assay stated on the supplied certificate of analysis, when available.
The boronic acid group is the main synthetic handle in this molecule. A common role for arylboronic acids is participation in palladium-catalyzed Suzuki–Miyaura cross-coupling, where an aryl group can be coupled with a suitable organic halide or related coupling partner. The specific catalyst, base, solvent, temperature, reaction time, and stoichiometry are selected for the full reaction system; there is no single set of conditions that can be assumed to work for every substrate.
The isopropyl group provides a defined substituent on the aromatic ring and remains part of the aryl fragment when that fragment is incorporated into a product. This can make the compound relevant when a target structure specifically calls for a para-isopropylphenyl unit. It should not be treated as interchangeable with phenylboronic acid or another substituted boronic acid, because changing the substituent changes the identity and properties of the resulting molecule.
These are potential synthetic contexts, not guarantees of reaction yield or suitability. Buyers should share the intended application and relevant technical requirements when requesting product information, particularly if the material will be used beyond exploratory laboratory work.
Core identity data can be stated from the molecular structure, but many purchasing specifications are batch-dependent. Appearance, assay, water content, impurity profile, and residual solvent information should be verified using the current product specification and batch documentation rather than inferred from the chemical name. If a particular test method or acceptance limit is necessary, buyers should define it before ordering.
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| Specification item | Why it matters | Buyer action |
|---|---|---|
| Identity | Confirms the material is the requested compound. | Check the product name, CAS number, and available analytical documentation. |
| Assay or purity | Supports quantity calculations and internal acceptance decisions. | Request the applicable limit and batch result; do not assume a value. |
| Appearance | Provides a basic description for receipt and inspection. | Confirm the stated description for the offered grade and lot. |
| Water and impurity profile | May be relevant to handling or a moisture-sensitive reaction. | Specify required tests and limits where the process calls for them. |
| Packaging and storage | Influence transport, containment, and material management. | Review the proposed pack size and follow the supplied SDS and label. |
Do not assume a particular melting point, solubility, shelf life, or storage temperature without a reliable product-specific document. Conditions can vary by grade, batch, packaging, or supplier guidance. For safe use, consult the safety data sheet and site procedures before opening or handling the material.
Start with the role the compound will play in your process. A small-scale route-screening study may have different documentation and quantity needs from a scale-up campaign or a controlled manufacturing process. Clarifying the application helps align the requested assay, impurity controls, packaging, and documentation with the actual acceptance criteria.
Supplier evaluation should focus on clear product identification, transparent batch documentation, communication about specification limits, and a practical response to logistics questions. If your organization requires a specific test method, audit documentation, or change-control information, raise that requirement during quotation rather than after order confirmation. These checks help reduce avoidable differences between a requested material and the material your team is prepared to receive.
Maison Chemical supplies chemicals for B2B buyers and can discuss 4-Isopropylbenzeneboronic acid CAS 16152-51-5 against your project requirements. For a useful quotation, provide the requested quantity, destination, target delivery window, and any required assay or documentation criteria. We can then confirm the applicable product information and commercial details for the offer.
Because availability, packaging, and batch specifications can change, buyers should verify current details before placing an order. Maison Chemical does not recommend treating general chemical identity data as a substitute for lot-specific documents or a formal product specification. For regulated or process-critical use, review the supplied documentation with your quality, safety, and technical teams.
4-Isopropylbenzeneboronic acid is an arylboronic acid with CAS 16152-51-5, formula C9H13BO2, and a molar mass of approximately 164.01 g/mol. Its principal value is as a potential synthetic building block for introducing a para-isopropylphenyl group, including in suitable Suzuki–Miyaura coupling routes. Whether it is appropriate for a specific synthesis depends on the target structure, reaction conditions, and required material quality.
As a next step, compare the identity data with your route specification, define the quality and documentation requirements, and request current batch and quotation details. Contact Maison Chemical with your quantity, destination, and technical criteria to discuss sourcing options. This approach gives your team a clear basis for evaluating the compound before purchase.
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