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269410-25-5

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269410-25-5 Usage

Description

2,6-DIMETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL is a white to beige crystalline powder with chemical properties that make it suitable for various applications in different industries.

Uses

Used in Chemical Synthesis:
2,6-DIMETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL is used as a chemical intermediate for the synthesis of various compounds due to its unique structure and reactivity.
Used in Pharmaceutical Industry:
2,6-DIMETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL is used as a building block for the development of new pharmaceutical compounds, potentially contributing to the creation of novel drugs with improved therapeutic properties.
Used in Material Science:
2,6-DIMETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL is used as a component in the development of advanced materials, such as polymers and composites, due to its structural characteristics and potential to enhance material properties.
Used in Research and Development:
2,6-DIMETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL is used as a research compound for studying its properties and potential applications in various fields, including chemistry, biology, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 269410-25-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,4,1 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 269410-25:
(8*2)+(7*6)+(6*9)+(5*4)+(4*1)+(3*0)+(2*2)+(1*5)=145
145 % 10 = 5
So 269410-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H21BO3/c1-9-7-11(8-10(2)12(9)16)15-17-13(3,4)14(5,6)18-15/h7-8,16H,1-6H3

269410-25-5 Well-known Company Product Price

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  • TCI America

  • (D2853)  2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol  >98.0%(GC)

  • 269410-25-5

  • 1g

  • 680.00CNY

  • Detail
  • TCI America

  • (D2853)  2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol  >98.0%(GC)

  • 269410-25-5

  • 5g

  • 2,560.00CNY

  • Detail
  • Aldrich

  • (518794)  4-Hydroxy-3,5-dimethylphenylboronicacidpinacolester  97%

  • 269410-25-5

  • 518794-1G

  • 616.59CNY

  • Detail
  • Aldrich

  • (518794)  4-Hydroxy-3,5-dimethylphenylboronicacidpinacolester  97%

  • 269410-25-5

  • 518794-5G

  • 2,465.19CNY

  • Detail

269410-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-DIMETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-3,5-dimethylphenylboronic Acid Pinacol Ester

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:269410-25-5 SDS

269410-25-5Relevant articles and documents

Bedford-type palladacycle-catalyzed miyaura borylation of aryl halides with tetrahydroxydiboron in water

Zernickel, Anna,Du, Weiyuan,Ghorpade, Seema A.,Sawant, Dinesh N.,Makki, Arwa A.,Sekar, Nagaiyan,Eppinger, J?rg

, p. 1842 - 1851 (2018/02/23)

A mild aqueous protocol for palladium catalyzed Miyaura borylation of aryl iodides, aryl bromides and aryl chlorides with tetrahydroxydiboron (BBA) as a borylating agent is developed. The developed methodology requires low catalyst loading of Bedford-type palladacycle catalyst (0.05 mol %) and works best under mild reaction conditions at 40 °C in short time of 6 h in water. In addition, our studies show that for Miyaura borylation using BBA in aqueous condition, maintaining a neutral reaction pH is very important for reproducibility and higher yields of corresponding borylated products. Moreover, our protocol is applicable for a broad range of aryl halides, corresponding borylated products are obtained in excellent yields up to 93% with 29 examples demonstrating its broad utility and functional group tolerance.

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