2066512-27-2

Basic information

• Product Name: 2-(diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 2066512-27-2
• Molecular Weight: 393.799
• Mol File: 2066512-27-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(2066512-27-2)
• EPA Substance Registry System: 2-(diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(2066512-27-2)

Safety Data

• Hazardous Substances Data: 2066512-27-2(Hazardous Substances Data)

Usage

General Description

2-(diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical compound with the molecular formula C10H18BIO2I2. It is a boronic ester that contains two iodomethyl groups and four methyl substituents. 2-(diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure and reactivity make it useful in the preparation of pharmaceuticals, agrochemicals, and materials science applications. Additionally, it is often utilized in the field of organic chemistry as a versatile building block for the preparation of complex molecules. However, it is important to handle this compound with care, as it is toxic and may present hazards to human health and the environment.

Upstream product

• 83622-41-7 pinacol dichloromethylboronic ester 
• 7681-82-5 sodium iodide 
• 76-09-5 2,3-dimethyl-2,3-butane diol 

Downstream Products

• 1240492-43-6 (±)-4,4,5,5-tetramethyl-2-[2-phenylcyclopropyl]-1,3,2-dioxaborolane 
• 1240492-43-6 racemic 4,4,5,5-tetramethyl-2-((1S,2S)-2-phenylcyclopropyl)-1,3,2-dioxaborolane 

Relevant articles and documents

MONOACYLGLYCEROL LIPASE MODULATORS

3.1.0 and 4.1.0 Azabicycle compounds of Formula (I), pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions associated with MGL modulation, su

Borocyclopropanation of Styrenes Mediated by UV-light Under Continuous Flow Conditions

Herein, we report a user-friendly and metal-free UV-A light mediated borocyclopropanation of styrenes using continuous flow technology. A broad range of styrene derivatives can be cyclopropanated in good yields within 1 h residence time to produce highly

Diastereoselective borocyclopropanation of allylic ethers using a boromethylzinc carbenoid

A borocyclopropanation of (E)- and (Z)-allylic ethers and styrene derivatives via the Simmons-Smith reaction using a novel boromethylzinc carbenoid is described. The carbenoid precursor is prepared via a 3-step sequence from inexpensive and commercially available starting materials. This methodology allows for the preparation of 1,2,3-substituted borocyclopropanes in high yields and diastereoselectivities. Several postfunction-alization reactions were also performed to illustrate the versatility of these building blocks.