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912824-84-1

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912824-84-1 Usage

General Description

2-(dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical compound commonly used in organic synthesis and medicinal chemistry. It is a boronic acid derivative that contains a dibenzo[b,d]thiophene group, as well as four methyl groups on the boron atom. 2-(dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is often used as a reagent in Suzuki coupling reactions, which are important in the synthesis of pharmaceuticals and other organic molecules. Additionally, the dibenzo[b,d]thiophene group in the compound is known for its biological activity and is found in a variety of natural products and pharmaceuticals. Therefore, 2-(dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile and important chemical in the fields of organic synthesis and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 912824-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,8,2 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 912824-84:
(8*9)+(7*1)+(6*2)+(5*8)+(4*2)+(3*4)+(2*8)+(1*4)=171
171 % 10 = 1
So 912824-84-1 is a valid CAS Registry Number.

912824-84-1 Well-known Company Product Price

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  • TCI America

  • (T3236)  4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzothiophene  >98.0%(GC)(T)

  • 912824-84-1

  • 1g

  • 590.00CNY

  • Detail
  • TCI America

  • (T3236)  4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzothiophene  >98.0%(GC)(T)

  • 912824-84-1

  • 5g

  • 1,990.00CNY

  • Detail

912824-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-dibenzothiophen-4-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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:912824-84-1 SDS

912824-84-1Relevant articles and documents

Engaging Ag(0) single atoms in silver(I) salts-mediated C-B and C-S coupling under visible light irradiation

Cui, Enxin,Qiao, Dan,Li, Haibin,Guo, Lirong,Tung, Chen-Ho,Wang, Yifeng

, p. 255 - 263 (2021/09/06)

Silver(I) salts were found active in the borylation and sulfenylation of aryl iodides under visible light irradiation. The optimized borylation protocol using AgF did not need any additive, operated under very mild conditions, and well tolerated a broad scope of substrates and boron sources. Formation of Ag(0) single atoms (AgSAs) during the borylation reactions was examined using high-angle annular dark field aberration-corrected scanning transmission electron microscope (HAADF AC-STEM) and electron paramagnetic resonance (EPR). The activities of the silver(I) salts were affected by the anions and could be associated with their abilities in formation of AgSAs during the reactions. Kinetic studies showed that the deiodination rate was linearly correlated with the loading of AgSAs, and hence AgSAs were the true catalytic centers for the 1e?-reduction of the C-I moieties. The oxidation state of AgSAs kept 0 in both the resting and the working states. A “work-in-tandem” mechanism involving AgSAs as the catalytic centers and AgNPs as the light absorber to achieve the borylation of aryl iodides under visible light irradiation is proposed. The current approach not only provides an alternative system for borylation and sulfenylation of aryl iodides, but also reveals a new activity of silver(I) salts involving AgSAs under visible light irradiation.

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

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Paragraph 0233-0237, (2020/07/29)

The present invention provides a compound of chemical formula 1 and an organic light emitting device comprising the same. The organic light emitting device containing the compound has excellent lifespan characteristics and can have high luminous efficiency even at a low driving voltage.COPYRIGHT KIPO 2020

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT USING SAME, AND ELECTRONIC DEVICE COMPRISING SAME ORGANIC ELECTRONIC ELEMENT

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Paragraph 0175; 0324-0325; 0332-0333, (2019/05/18)

Provided are an organic electric element and an electronic device comprising the same. According to the present invention, the organic electric element uses a mixture of compounds as a phosphorescent host material which can achieve a high light-emitting efficiency and a low driving voltage and can greatly improve a lifespan in an organic electric element.

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