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2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boronic acid derivative with the molecular formula C14H16BF2O2. It is a colorless liquid that is stable under normal conditions and is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction, a powerful method for forming carbon-carbon bonds. The unique structure of 2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane makes it a valuable building block for the synthesis of complex organic molecules.

881402-15-9

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881402-15-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent in the synthesis of pharmaceutical compounds for its ability to facilitate the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction. This reaction is crucial for the creation of complex organic molecules that can be used as active pharmaceutical ingredients.
Used in Materials Science:
In the field of materials science, 2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a building block for the development of new materials with specific properties. Its role in the Suzuki-Miyaura cross-coupling reaction allows for the creation of novel polymers and other materials with tailored characteristics for various applications.
Used in Agrochemicals:
2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is utilized in the agrochemical industry as a reagent for the synthesis of new agrochemical compounds. The Suzuki-Miyaura cross-coupling reaction it enables is essential for the development of innovative pesticides, herbicides, and other agrochemicals that can improve crop protection and yield.
Overall, the versatility of 2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in organic synthesis and its applications across different industries highlight its importance as a key chemical compound in modern science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 881402-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,4,0 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 881402-15:
(8*8)+(7*8)+(6*1)+(5*4)+(4*0)+(3*2)+(2*1)+(1*5)=159
159 % 10 = 9
So 881402-15-9 is a valid CAS Registry Number.

881402-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 2-[2,3-difluoro-4-(trifluoromethyl)phenyl]-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:881402-15-9 SDS

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