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(4-Formyl-1-naphthalene)boronic acid, with the molecular formula C12H9BO3, is a boronic acid derivative featuring a naphthalene ring and a formyl group. It is a versatile chemical compound that plays a significant role in organic synthesis and chemical research.

332398-52-4

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332398-52-4 Usage

Uses

Used in Organic Synthesis:
(4-Formyl-1-naphthalene)boronic acid is used as a reagent in the Suzuki-Miyaura coupling reaction, a widely employed method for creating carbon-carbon bonds. This reaction is crucial for the construction of complex organic molecules, making the compound an essential tool in this field.
Used in Pharmaceutical Industry:
(4-Formyl-1-naphthalene)boronic acid is utilized in the development of pharmaceuticals due to its ability to form carbon-carbon bonds, which is vital for the synthesis of various drug molecules. Its applications in this industry contribute to the advancement of new and improved medications.
Used in Materials Science:
(4-FORMYL-1-NAPHTHALENE)BORONIC ACID is also employed in the materials science industry, where its properties are harnessed for the development of new materials with specific characteristics. Its involvement in this field aids in the creation of innovative materials with potential applications in various sectors.
Used in Sensor and Optical Material Development:
(4-Formyl-1-naphthalene)boronic acid is known for its fluorescent properties, making it a valuable component in the development of sensors and optical materials. Its use in these applications allows for the creation of highly sensitive and efficient devices and materials for various purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 332398-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,3,9 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 332398-52:
(8*3)+(7*3)+(6*2)+(5*3)+(4*9)+(3*8)+(2*5)+(1*2)=144
144 % 10 = 4
So 332398-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BO3/c13-7-8-5-6-11(12(14)15)10-4-2-1-3-9(8)10/h1-7,14-15H

332398-52-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H53143)  4-Formylnaphthalene-1-boronic acid, 95%   

  • 332398-52-4

  • 250mg

  • 4168.0CNY

  • Detail

332398-52-4SDS

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 (4-formylnaphthalen-1-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-Formylnaphthalene-1-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:332398-52-4 SDS

332398-52-4Upstream product

332398-52-4Relevant academic research and scientific papers

Photochromism of a radical diffusion-inhibited hexaarylbiimidazole derivative with intense coloration and fast decoloration performance

Fujita, Kana,Hatano, Sayaka,Kato, Daisuke,Abe, Jiro

supporting information; experimental part, p. 3105 - 3108 (2009/05/07)

(Figure Presented) We report the synthesis and the photochromic behavior of a newly designed, photochromic, radical diffusion-inhibited hexaarylbiimidazole (HABI) derivative with markedly improved photochromic performance in coloration and decoloration rates as well as greater optical density in the colored state. The thermal bleaching rate (τ1/2 = 260 ms at 295 K) is the fastest among the reported ones for HABI derivatives.

PIPERAZINE DERIVATIVES AS 5-HT1B ANTAGONISTS

-

Page 10, (2010/11/30)

Piperazine derivatives of formula(1),processes for their preparation, pharmaceutical compositions containing them in the treatment of CNS and other disorders and in their use in therapy as 5-HT1B antagonists are disclosed herein.

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