Description

4,6-Methano-1,3,2-Benzodioxaborole, Hexahydro-3A,5,5-Trimethyl-2-(3-Methylbutyl)-, [3As-(3Aα,4β,6β,7Aα)]- (9Ci) is a specialized organoboron compound of significant interest in advanced synthetic chemistry. This chemical serves as a versatile building block and reagent, enabling precise molecular transformations that are difficult to achieve with other materials. It is primarily needed by pharmaceutical R&D teams, agrochemical manufacturers, and academic research institutions developing novel active ingredients and functional materials.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of complex drug candidates, particularly those requiring boron-containing pharmacophores.
• Agrochemical Synthesis: Used in creating novel pesticides and herbicides with specific modes of action.
• Cross-Coupling Reactions: Acts as a boron reagent in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions for C-C bond formation.
• Material Science Research: Employed in the development of organic electronic materials and boron-doped polymers.
• Asymmetric Catalysis: Serves as a chiral ligand or auxiliary in stereoselective synthesis.
• Academic & Process Chemistry: A valuable tool for method development and exploring new synthetic pathways in laboratory settings.

Basic Information

Product Name	4,6-Methano-1,3,2-Benzodioxaborole, Hexahydro-3A,5,5-Trimethyl-2-(3-Methylbutyl)-, [3As-(3Aα,4β,6β,7Aα)]- (9Ci)
CAS No.	84110-39-4
Molecular Formula	C15H27BO2
Molecular Weight	250.19 g/mol
Synonyms	Hexahydro-3a,5,5-trimethyl-2-(3-methylbutyl)-4,6-methano-1,3,2-benzodioxaborole; 2-(3-Methylbutyl)-4,6-methano-1,3,2-benzodioxaborolane, hexahydro-3a,5,5-trimethyl-; Pinanediol 3-Methylbutylboronate; 3-Methylbutylboronic Acid Pinanediol Ester; (3-Methylbutyl)boronic Acid Pinacol Ester (common misnomer); Neopentyl Glycol Derived Boronate Ester; B-(3-Methylbutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (structural analog).
EINECS	Contact for details

Quality Control

Our production of this organoboron compound adheres to strict quality management protocols to ensure batch-to-batch consistency and high purity. All materials are characterized using advanced analytical techniques including NMR, HPLC, and GC. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment to support your quality assurance and regulatory needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic and easily oxidized nature, it is recommended to store the product under an inert atmosphere (e.g., nitrogen or argon) for long-term preservation. Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC/HPLC)	≥ 95.0%
Water Content (KF)	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.