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2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing chemical compound that is part of the family of organic synthesis molecules. It features a unique structure with a boron atom, a phenyl ring, and a dioxaborolane ring, which enables it to engage in a variety of chemical reactions. This versatile compound is particularly valuable in the fields of drug discovery and development, as well as materials science and catalysis, due to its potential to create new compounds with medicinal properties and its boron-containing core.

959972-40-8

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959972-40-8 Usage

Uses

Used in Organic Synthesis:
2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of new compounds with potential applications in different industries.
Used in Drug Discovery and Development:
In the pharmaceutical industry, 2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a key intermediate in the synthesis of drug candidates. Its unique structure allows for the development of compounds with potential medicinal properties, contributing to the advancement of new treatments and therapies.
Used in Materials Science:
2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is utilized as a component in the development of new materials, thanks to its boron-containing core. This makes it a valuable asset in the creation of innovative materials with unique properties for various applications.
Used in Catalysis:
In the field of catalysis, 2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is employed as a catalyst or a catalyst precursor. Its involvement in chemical reactions can enhance the efficiency and selectivity of processes, making it a useful tool for improving industrial chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 959972-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,9,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 959972-40:
(8*9)+(7*5)+(6*9)+(5*9)+(4*7)+(3*2)+(2*4)+(1*0)=248
248 % 10 = 8
So 959972-40-8 is a valid CAS Registry Number.

959972-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-(2-methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names -

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:959972-40-8 SDS

959972-40-8Relevant academic research and scientific papers

Chemoselective, Scalable Nickel-Electrocatalytic O-Arylation of Alcohols

Baran, Phil S.,Chen, Longrui,Edwards, Jacob T.,Kawamata, Yu,Oderinde, Martins S.,Zhang, Hai-Jun

supporting information, p. 20700 - 20705 (2021/08/17)

The formation of aryl-alkyl ether bonds through cross coupling of alcohols with aryl halides represents a useful strategic departure from classical SN2 methods. Numerous tactics relying on Pd-, Cu-, and Ni-based catalytic systems have emerged over the past several years. Herein we disclose a Ni-catalyzed electrochemically driven protocol to achieve this useful transformation with a broad substrate scope in an operationally simple way. This electrochemical method does not require strong base, exogenous expensive transition metal catalysts (e.g., Ir, Ru), and can easily be scaled up in either a batch or flow setting. Interestingly, e-etherification exhibits an enhanced substrate scope over the mechanistically related photochemical variant as it tolerates tertiary amine functional groups in the alcohol nucleophile.

1,5,7-TRISUBSTITUTED ISOQUINOLINE DERIVATIVES, PREPARATION THEREOF, AND USE THEREOF IN MEDICINES

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Paragraph 0230; 0232; 0234, (2020/08/30)

The present disclosure relates to 1,5,7-trisubstituted isoquinoline derivatives, their preparation and pharmaceutical use. In particular, the present disclosure discloses a compound of formula (I) or a pharmaceutically acceptable salt, stereoisomer, solvate or prodrug thereof, and a preparation method and use thereof. The definitions of the groups in the formula can be found in the specification and claims.

INHIBITORS OF FIBROBLAST ACTIVATION PROTEIN

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Paragraph 0227, (2020/07/14)

Compounds and compositions for modulating fibroblast activation protein (FAP) are described. The compounds and compositions may find use as therapeutic agents for the treatment of diseases, including hyperproliferative diseases.

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

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Paragraph 0154; 0155, (2014/05/08)

Provided are pyridopyrazine compounds of formula (1), pharmaceutical compositions thereof and methods of use therefore, wherein R1, R2, R3, R4 and m are as defined in the specification.

HERBICIDAL COMPOUNDS

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Page/Page column 38, (2014/09/29)

The present invention relates to compounds of Formula (I), or an agronomically acceptable salt of said compounds wherein A1, A2, A3, X1, X2, R1, R2 and R4 are as defined herein. The invention further relates to herbicidal compositions which comprise a compound of Formula (I), to their use for controlling weeds, in particular in crops of useful plants, and to intermediates used to synthesise said compounds.

Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors

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Page/Page column 107; 108, (2013/03/26)

Disclosed herein are compounds of Formula (II) that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical c

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

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Page/Page column 33-34, (2013/02/27)

Provided are certain pyridopyrazine compounds, pharmaceutical compositions thereof and methods of use therefor.

Pyrimidine compounds and methods of making and using same

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Page/Page column 75-76, (2013/02/27)

Disclosed herein are pyrimidinyl compounds that are contemplated to be modulators of cystic fibrosis transmembrane regulators (CFTR), and methods of making and using same. Also provided are pharmaceutical compositions and methods of treating disorders associated with cystic fibrosis transmembrane regulators, such as airway inflammation, cystic fibrosis, and the like.

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