Description
4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (CAS No. 882670-69-1) is a highly versatile boronic ester derivative with the molecular formula C13H20BNO2. This compound features a reactive boronate group protected by a pinacol ester, making it an excellent intermediate for Suzuki-Miyaura cross-coupling reactions and other palladium-catalyzed transformations. The aniline moiety further enhances its utility in pharmaceutical and agrochemical synthesis. With a purity of ≥95% (typical), this reagent is supplied as a crystalline solid, ensuring consistent performance in research and industrial applications. Ideal for use in medicinal chemistry, material science, and catalysis, it is packaged under inert conditions to maintain stability and shelf life.
Properties
- CAS Number: 882670-69-1
- Complexity: 277
- IUPAC Name: 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
- InChI: InChI=1S/C13H20BNO2/c1-9-6-7-10(15)8-11(9)14-16-12(2,3)13(4,5)17-14/h6-8H,15H2,1-5H3
- InChI Key: HPNBWHDRLCVZFV-UHFFFAOYSA-N
- Exact Mass: 233.1587090
- Molecular Formula: C13H20BNO2
- Molecular Weight: 233.12
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C(C=CC(=C2)N)C
- Topological: 44.5
- Monoisotopic Mass: 233.1587090
- Synonyms: 882670-69-1, 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, DTXSID80582076, DTXCID50532841, 623-049-5, 5-AMINO-2-METHYLPHENYLBORONIC ACID, PINACOL ESTER, 5-Amino-2-methylphenylboronic acid pinacol ester, MFCD05663859, 4-METHYL-3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZENAMINE, SCHEMBL393594, (5-AMINO-2-METHYLPHENYL)BORONIC ACID PINACOL ESTER, 4-methyl-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, HPNBWHDRLCVZFV-UHFFFAOYSA-N, BCP15006, BBL101705, STL555501, AKOS007930614, AB21963, BENZENAMINE, 4-METHYL-3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-, NCGC00662711-01, DS-14908, CS-0030610, EN300-371885, 5-amino-2-methyl-phenylboronic acid pinacol ester, 5-Amino-2-methylphenylboronic acid pinacol ester, 97%, Z2044807984
Application
This compound is widely used as a key intermediate in the synthesis of bioactive molecules, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient cross-coupling reactions for constructing complex aromatic systems. Researchers also utilize it in the preparation of fluorescent dyes and advanced materials. The aniline functionality allows for further derivatization, expanding its applications in drug discovery.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statements
- P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2 (100%)
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