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5-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a complex organic compound with the molecular formula C14H19BO3. It is a derivative of phenol, featuring a methyl group at the 5th position and a tetramethyl-1,3,2-dioxaborolane group at the 2nd position. 5-Methyl-2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenol is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are a type of carbon-carbon bond-forming reaction. The tetramethyl-1,3,2-dioxaborolane group acts as a boron-based nucleophile, facilitating the coupling of the phenol with other organic molecules. Its stability and reactivity make it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.

517864-13-0

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517864-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 517864-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,7,8,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 517864-13:
(8*5)+(7*1)+(6*7)+(5*8)+(4*6)+(3*4)+(2*1)+(1*3)=170
170 % 10 = 0
So 517864-13-0 is a valid CAS Registry Number.

517864-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

1.2 Other means of identification

Product number -
Other names PHENOL,5-METHYL-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)

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:517864-13-0 SDS

517864-13-0Relevant academic research and scientific papers

Ruthenium-catalyzed regio- And site-selective: Ortho C-H borylation of phenol derivatives

Homma, Yuki,Fukuda, Kazuishi,Iwasawa, Nobuharu,Takaya, Jun

supporting information, p. 10710 - 10713 (2020/10/02)

Efficient synthesis of o-borylphenols is achieved through the Ru-catalyzed regio- and site-selective sp2 C-H borylation of aryl diphenylphosphinites followed by removal of the phosphorus directing group. A successful application to aryl phosphites enables practical one-pot borylation of phenols, demonstrating high synthetic utility of this protocol.

Regioselective Synthesis of o-Benzenediboronic Acids via Ir-Catalyzed o-C-H Borylation Directed by a Pyrazolylaniline-Modified Boronyl Group

Yamamoto, Takeshi,Ishibashi, Aoi,Suginome, Michinori

supporting information, p. 886 - 889 (2017/02/26)

Ir-catalyzed ortho-directed C-H borylation of pyrazolylaniline (PZA)-modified arylboronic acids with bis(pinacolate)diboron afforded o-benzenediboronic acids in which two boronyl groups are differentially modified by pinacol (PIN) and PZA. By using this borylation after nondirected Ir-catalyzed C-H borylation, o-benzenediboronic acids are conveniently synthesized from unfunctionalized arenes. The differentially modified o-benzenediboronic acids undergo selective oxidation and Suzuki-Miyaura cross-coupling at the PZA-modified boronyl groups, affording o-functionalized arylboronic acids selectively.

CRYSTALLINE ANTI-TRICHOPHYTON AGENTS AND PREPARATION PROCESS THEREOF

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Paragraph 0093; 0094, (2017/09/02)

A crystal form of 2-(3,5-dimethyl-1H-pyrazol-1-yl)-5-methylphenol which is stable and has high purity for preservation, industrial manufacturing, and circulation, and process for providing the same by using a boron compound.

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