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174090-36-9

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174090-36-9 Usage

General Description

4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolane is a chemical compound with the molecular formula C14H21BO2. It is a boronic ester, which is commonly used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-oxygen bonds. 4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolane is a colorless liquid and is highly stable under normal conditions. It is often utilized in pharmaceutical research, as well as in the development of agrochemicals and materials science. 4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolane is considered to be a valuable building block in the production of various functional molecules and is an important tool in modern chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 174090-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 174090-36:
(8*1)+(7*7)+(6*4)+(5*0)+(4*9)+(3*0)+(2*3)+(1*6)=129
129 % 10 = 9
So 174090-36-9 is a valid CAS Registry Number.

174090-36-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-Tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names (1-Phenethyl)pinacolboronate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:174090-36-9 SDS

174090-36-9Relevant articles and documents

Electrosynthesis of benzylboronic acids and esters

Pintaric,Laza,Olivero,Du?ach

, p. 8031 - 8033 (2004)

A novel preparation of benzylboronic acids and esters is described by using an electrochemical reductive coupling reaction between benzylic halides and borating agents (trialkylborates or pinacolborane). The reaction is carried out at room temperature in DMF or THF with the use of a sacrificial magnesium anode in a single-compartment cell.

Selective Benzylic CH-Borylations by Tandem Cobalt Catalysis

Bauer, Matthias,Ghosh, Pradip,Jacobi von Wangelin, Axel,Schoch, Roland

supporting information, (2021/11/27)

Metal-catalyzed C?H activations are environmentally and economically attractive synthetic strategies for the construction of functional molecules as they obviate the need for pre-functionalized substrates and minimize waste generation. Great challenges reside in the control of selectivities, the utilization of unbiased hydrocarbons, and the operation of atom-economical dehydrocoupling mechanisms. An especially mild borylation of benzylic CH bonds was developed with the ligand-free pre-catalyst Co[N(SiMe3)2]2 and the bench-stable and inexpensive borylation reagent B2pin2 that produces H2 as the only by-product. A full set of kinetic, spectroscopic, and preparative mechanistic studies are indicative of a tandem catalysis mechanism of CH-borylation and dehydrocoupling via molecular CoI catalysts.

Selective electrocatalytic hydroboration of aryl alkenes

Zhang, Yahui,Zhao, Xiangyu,Bi, Ce,Lu, Wenqi,Song, Mengyuan,Wang, Dongdong,Qing, Guangyan

, p. 1691 - 1699 (2021/03/09)

Organoboron compounds are powerful precursors of value-added organic compounds in synthetic chemistry, and transition metal-catalysed borylation has always been dominant. To avoid toxic reagents and costs associated with metal catalysts, simpler, more eco

Manganese-Catalyzed Hydroboration of Terminal Olefins and Metal-Dependent Selectivity in Internal Olefin Isomerization-Hydroboration

Garhwal, Subhash,Kroeger, Asja A.,Thenarukandiyil, Ranjeesh,Fridman, Natalia,Karton, Amir,De Ruiter, Graham

supporting information, p. 494 - 504 (2021/01/11)

In the past decade, the use of earth-abundant metals in homogeneous catalysis has flourished. In particular, metals such as cobalt and iron have been used extensively in reductive transformations including hydrogenation, hydroboration, and hydrosilylation

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