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9-ethyl-3-carbazole boronic acid is a chemical compound characterized by the molecular formula C14H14BNO2. It is recognized for its boronic acid functional group and the carbazole moiety, which endows it with unique photophysical and electronic properties. 9-ethyl-3-carbazole boronic acid is widely regarded as a valuable building block in the realms of organic synthesis and medicinal chemistry, particularly due to its utility in Suzuki-Miyaura coupling reactions for carbon-carbon bond formation.

669072-93-9

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669072-93-9 Usage

Uses

Used in Organic Synthesis:
9-ethyl-3-carbazole boronic acid is used as a building block for the synthesis of various organic compounds. Its boronic acid functional group plays a crucial role in facilitating Suzuki-Miyaura coupling reactions, which are essential for the formation of carbon-carbon bonds in organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 9-ethyl-3-carbazole boronic acid is utilized for the development of pharmaceutical agents. Its unique structure and properties make it a promising candidate for the synthesis of new drugs with potential therapeutic applications.
Used in Optoelectronic Devices:
9-ethyl-3-carbazole boronic acid is used as a component in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. The carbazole moiety in the molecule contributes to its photophysical properties, making it suitable for applications that require light emission or electronic conductivity.
Used in Materials Science:
9-ethyl-3-carbazole boronic acid is also employed in materials science for the creation of new materials with specific properties. Its versatility and the ability to form carbon-carbon bonds through Suzuki-Miyaura coupling reactions make it an asset in the design and synthesis of advanced materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 669072-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,0,7 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 669072-93:
(8*6)+(7*6)+(6*9)+(5*0)+(4*7)+(3*2)+(2*9)+(1*3)=199
199 % 10 = 9
So 669072-93-9 is a valid CAS Registry Number.

669072-93-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H64959)  9-Ethylcarbazole-3-boronic acid, 98%   

  • 669072-93-9

  • 250mg

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64959)  9-Ethylcarbazole-3-boronic acid, 98%   

  • 669072-93-9

  • 1g

  • 588.0CNY

  • Detail
  • Alfa Aesar

  • (H64959)  9-Ethylcarbazole-3-boronic acid, 98%   

  • 669072-93-9

  • 5g

  • 2352.0CNY

  • Detail

669072-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-Ethyl-3-Carbazole Boronic Acid

1.2 Other means of identification

Product number -
Other names (9-ethylcarbazol-3-yl)boronic acid

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:669072-93-9 SDS

669072-93-9Relevant academic research and scientific papers

5-(Methylidene)barbituric acid as a new anchor unit for dye-sensitized solar cells (DSSC)

Irgashev, Roman A.,Kim, Grigory A.,Rusinov, Gennady L.,Charushin, Valery N.

, p. 123 - 131 (2014)

Novel dyes bearing a 5-(methylidene)barbituric acid moiety as a new acceptor/anchor fragment were obtained and exhibited remarkable photophysical properties, according to a preliminary assessment of their sensitization activity as elements for dye-sensitized solar cells. ARKAT-USA, Inc.

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