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4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine is a complex chemical compound featuring a pyridine ring connected to a phenyl group, which is further linked to a boron-containing dioxaborolane ring. The dioxaborolane ring is a five-membered heterocyclic structure with both boron and oxygen atoms, and the tetramethyl groups attached to it provide steric hindrance, potentially affecting the compound's reactivity and stability. 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine may find applications in various chemical reactions, including organic synthesis, materials science, and pharmaceutical research. Due to its potential reactivity and toxicity, it is crucial to handle and use 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine with appropriate safety measures.

1009033-83-3

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1009033-83-3 Usage

Uses

Used in Organic Synthesis:
4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, enabling the synthesis of a wide range of molecules with potential applications in different industries.
Used in Materials Science:
In the field of materials science, 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine is used as a building block for the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with improved characteristics, such as enhanced stability, reactivity, or selectivity.
Used in Pharmaceutical Research:
4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine is utilized as a key component in the design and synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a valuable candidate for the development of new drugs with potential therapeutic applications. Researchers can exploit its properties to create molecules with specific biological activities, targeting various diseases and medical conditions.
Used in Chemical Reactions:
4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine is employed as a reactant in various chemical reactions, such as cross-coupling reactions, where it can be used to form new carbon-carbon or carbon-heteroatom bonds. Its reactivity and the presence of the boron-containing dioxaborolane ring make it a suitable candidate for these types of reactions, facilitating the synthesis of complex molecules with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1009033-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,0,3 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1009033-83:
(9*1)+(8*0)+(7*0)+(6*9)+(5*0)+(4*3)+(3*3)+(2*8)+(1*3)=103
103 % 10 = 3
So 1009033-83-3 is a valid CAS Registry Number.

1009033-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine

1.2 Other means of identification

Product number -
Other names 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine

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:1009033-83-3 SDS

1009033-83-3Relevant academic research and scientific papers

A pyridine phongl as the nuclear in the three compounds and methods for their preparation and use

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, (2016/11/02)

The invention belongs to the technical field of organic electroluminescence materials, and discloses a compound using tripyridylbenzene as a core as well as a preparation method and application thereof. The compound can be prepared by synthesizing a halog

QUINOXALINE DERIVATIVES AND ORGANIC LIGHT-EMITTING DIODES COMPRISING THE SAME

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, (2012/12/14)

A quinoxaline derivative represented by Formula (I) of or Formula (II) of is provided. In Formula (I) or (II), R1, R2, R3 and R4 are, independently, hydrogen, halogen, methyl, ethyl, propyl, butyl, aryl or heteroaryl, for example phenyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl or benzoimidazolyl. The disclosure also provides an organic light-emitting diode including the quinoxaline derivative.

Novel four-pyridylbenzene-armed biphenyls as electron-transport materials for phosphorescent OLEDs

Su, Shi-Jian,Tanaka, Daisaku,Li, Yan-Jun,Sasabe, Hisahiro,Takeda, Takashi,Kido, Junji

supporting information; experimental part, p. 941 - 944 (2009/04/07)

A series of four-pyridylbenzene-armed biphenyl derivatives were designed and synthesized as an electron-transport and exciton- and hole-block layer for the fac-tris(2-phenylpyridine)iridium (lr(PPy)3)-based green phosphorescent organic light-em

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