2,4-Dibutoxyphenylboronic acid
2,4-Dibutoxyphenylboronic acid (CAS: 870778-89-5) is a disubstituted aryl boronic acid derivative, primarily utilised as a reactant in organic synthesis. Its molecular structure, C14H23BO4, lends itself to sophisticated chemical reactions. This compound is particularly noted for its role in the synthesis of novel phenoxazine dyes and donors, which are essential components in the development of dye-sensitized solar cells, contributing to advancements in renewable energy technologies.
- Synonyms
- 2,4-Dibutoxyphenylboronic acidC14H23BO4

Phenoxazine Dye Synthesis
Serves as a key reactant in the synthesis of phenoxazine dyes, which are critical for the performance of dye-sensitized solar cells.
Donor Chromophore Development
Utilised in the synthesis of donors for chromophores, enabling the study and enhancement of spectral characteristics for dye-sensitized solar cell applications.
Organic Synthesis Intermediate
A versatile building block in organic chemistry for creating complex molecular structures, particularly those involving aryl boronic acid functionalities.
| Molecular weight | 266.14 |
|---|---|
| Empirical formula | C14H23BO4 |
| Application | Reactant for:• Synthesis of phenoxazine dyes for dye-sensitized solar cells1• Sythesis of donors for comparison of structural and spectral characteristics of chromophores for dye-sensitized solar cells2 |
| Melting point | 99-104 °C |
Hazard statements
- H413May cause long-lasting harmful effects to aquatic life
| Water hazard class (WGK, DE) | 3 |
|---|
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
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 2,4-Dibutoxyphenylboronic acid used for?
+
2,4-Dibutoxyphenylboronic acid is used as a reactant in the synthesis of phenoxazine dyes and donors for dye-sensitized solar cells, and as a general intermediate in organic synthesis.
What is the CAS number and formula for 2,4-Dibutoxyphenylboronic acid?
+
The CAS number for 2,4-Dibutoxyphenylboronic acid is 870778-89-5 and its molecular formula is C14H23BO4.
What is the purity or grade of this product?
+
This product is typically supplied at a research or technical grade. The exact assay is not specified, but it is suitable for chemical synthesis applications.
What are the safety considerations for 2,4-Dibutoxyphenylboronic acid?
+
According to GHS classifications, this compound may cause long lasting harmful effects to aquatic life (H413). Appropriate handling procedures should be followed.
How is 2,4-Dibutoxyphenylboronic acid packaged and shipped?
+
As a specialist global supplier, Tech Serve Solutions ensures that 2,4-Dibutoxyphenylboronic acid is securely packaged and exported in compliance with all relevant regulations for chemical transportation.
How can I request a quote for 2,4-Dibutoxyphenylboronic acid?
+
To request a quote, please contact our sales team via the website or direct email, providing the product name and CAS number (870778-89-5).
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis