Cas no 97571-07-8 (1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)-)

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)- is a highly stable boronic ester derivative commonly used in Suzuki-Miyaura cross-coupling reactions. Its sterically hindered structure, featuring tetramethyl substitution on the dioxaborolane ring and a bulky neopentyl-like substituent, enhances stability against hydrolysis and oxidative degradation. This compound is particularly valuable in organic synthesis, offering improved handling and storage characteristics compared to more labile boronic acids. Its consistent reactivity profile makes it a reliable reagent for constructing complex molecular architectures, particularly in pharmaceutical and materials science applications. The product's robustness under ambient conditions reduces the need for stringent storage requirements while maintaining high purity and reactivity in coupling reactions.

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)- structure

97571-07-8 structure

Product Name:1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)-

CAS No:97571-07-8

MF:C₁₂H₂₅BO₂

MW:212.136704206467

MDL:MFCD31390452

CID:4368286

Update Time:2025-05-21

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)- Chemical and Physical Properties

Names and Identifiers

- 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)-
- 2-(3,3-dimethylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- Reaxys ID: 17301523
- 2-(3,3-dimethylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(WXC07810)
- MDL： MFCD31390452
- Inchi： 1S/C12H25BO2/c1-9(10(2,3)4)13-14-11(5,6)12(7,8)15-13/h9H,1-8H3
- InChI Key： DAUZUYZUKDTCGK-UHFFFAOYSA-N
- SMILES： O1C(C)(C)C(C)(C)OB1C(C)C(C)(C)C

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)- Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1750839-1g	2-(3,3-Dimethylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane	97571-07-8	98%	1g	￥14984.00	2024-04-23
AstaTech	W13785-0.25/G	2-(3,3-DIMETHYLBUTAN-2-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE	97571-07-8	95%	0.25g	$618	2023-09-19
AstaTech	W13785-1/G	2-(3,3-DIMETHYLBUTAN-2-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE	97571-07-8	95%	1g	$1545	2023-09-19
Ambeed	A992113-1g	2-(3,3-Dimethylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane	97571-07-8	95%	1g	$2008.0	2025-04-14
Ambeed	A992113-250mg	2-(3,3-Dimethylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane	97571-07-8	95%	250mg	$803.0	2025-04-14

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)- Suppliers

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(CAS:97571-07-8)1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)-

Order Number:A1070292

Stock Status:in Stock

Quantity:1g

Purity:99%

Pricing Information Last Updated:Thursday, 29 August 2024 18:44

Price ($):1376.0

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Additional information on 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)-

1,3,2-Dioxaborolane, 4,4,5,5-Tetramethyl-2-(1,2,2-TriMethylPropyl)-: A Comprehensive Overview

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1,2,2-trimethylpropyl)- (CAS No: 97571-07-8) is a versatile organoborane compound that has garnered significant attention in the fields of organic synthesis and materials science. This compound is a derivative of dioxaborolane with a unique structure that incorporates multiple methyl groups and a bulky substituent at the 2-position. Its structure endows it with distinctive chemical properties and reactivity patterns.

The molecular structure of 1,3,2-dioxaborolane is characterized by a three-membered ring consisting of two oxygen atoms and one boron atom. The ring is further substituted with four methyl groups at positions 4 and 5 and a bulky 1,2,2-trimethylpropyl group at position 2. This substitution pattern significantly influences the compound's electronic properties and reactivity. Recent studies have highlighted its potential as a precursor in the synthesis of advanced materials and functional molecules.

One of the most notable applications of CAS No: 97571-07-8 is its role in the synthesis of highly functionalized boron-containing polymers. Researchers have demonstrated that this compound can undergo polymerization under specific conditions to yield materials with exceptional thermal stability and mechanical properties. These polymers have potential applications in aerospace engineering and high-performance electronics.

In addition to polymer synthesis,1,3,2-dioxaborolane has been explored as a catalyst in various organic transformations. Its ability to stabilize reactive intermediates makes it an attractive candidate for asymmetric catalysis and enantioselective reactions. Recent advancements in this area have leveraged its unique electronic properties to achieve unprecedented levels of enantioselectivity in key industrial processes.

The synthesis of CAS No: 97571-07-8 involves a multi-step process that typically begins with the reaction of trimethylborate with appropriate diols or glycols under acidic or basic conditions. The reaction conditions are critical to ensure high yields and purity of the final product. Innovations in this synthetic pathway have significantly improved the scalability and cost-effectiveness of producing this compound on an industrial scale.

From an environmental perspective,4,4,5-tetramethyl-dioxaborolane exhibits favorable biodegradation characteristics under controlled conditions. Studies have shown that it can be safely disposed of through conventional waste management practices without posing significant risks to ecosystems or human health.

In conclusion, CAS No: 97571-07-8, also known as 1,3,dioxaborolane, stands as a testament to the ingenuity of modern chemical synthesis and its applications across diverse industries.

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