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69807-91-6

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  • Factory Price OLED 99% 69807-91-6 3,5-Bis(trifluoroMethyl)phenylboronic acid pinacol ester Manufacturer

    Cas No: 69807-91-6

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69807-91-6 Usage

General Description

3,5-Bis(trifluoroMethyl)phenylboronic acid pinacol ester is a chemical compound that is a derivative of phenylboronic acid. It is commonly used in organic synthesis as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. It is also employed in the Suzuki-Miyaura coupling reaction, a widely-used method for creating biaryl compounds. 3,5-Bis(trifluoroMethyl)phenylboronic acid pinacol ester is a colorless solid with a molecular formula of C14H13BF6O2 and a molecular weight of 306.07 g/mol. It is a versatile and important reagent in the field of organic chemistry, with various potential applications in drug discovery and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 69807-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,0 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69807-91:
(7*6)+(6*9)+(5*8)+(4*0)+(3*7)+(2*9)+(1*1)=176
176 % 10 = 6
So 69807-91-6 is a valid CAS Registry Number.

69807-91-6 Well-known Company Product Price

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  • TCI America

  • (B5095)  2-[3,5-Bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane  >98.0%(GC)(T)

  • 69807-91-6

  • 1g

  • 450.00CNY

  • Detail
  • TCI America

  • (B5095)  2-[3,5-Bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane  >98.0%(GC)(T)

  • 69807-91-6

  • 5g

  • 1,550.00CNY

  • Detail

69807-91-6SDS

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 2-[3,5-bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC ACID PINACOL ESTER

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:69807-91-6 SDS

69807-91-6Relevant articles and documents

Cu-mediated: vs. Cu-free selective borylation of aryl alkyl sulfones

Hu, Jiefeng,Huang, Mingming,Marder, Todd B.,Radius, Udo,Tang, Man,Westcott, Stephen A.

supporting information, p. 395 - 398 (2022/01/19)

A Cu-catalysed borylation of aryl alkyl sulfones was developed for the high yield synthesis of versatile arylboronic esters using a readily prepared NHC-Cu catalyst. In addition, the selective cleavage of either alkyl(C)-sulfonyl or aryl(C)-sulfonyl bonds

Organic compound and electroluminescent device using same

-

Paragraph 0065-0067; 0111-0113, (2021/01/29)

The present invention provides an organic compound and an electroluminescent device using the same. The organic compound has a structure represented by a formula I, and the organic compound provided by the present invention is a D-carbazole-A configuratio

Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction

Boontiem, Phongsakorn,Kiatisevi, Supavadee

, (2020/03/03)

Facile and economical method for Miyaura borylation reaction between B2pin2 and aryl bromides is reported. The catalytic system containing 2 mol% PdCl2(PPh3)2 and KOAc serves to enable borylations to occur under solvent-free and atmospheric conditions. The developed protocol can be applied to synthesize symmetrical and unsymmetrical biaryls via one-pot two-step Suzuki–Miyaura cross-coupling reaction and also offers the up-scalability.

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