Welcome to LookChem.com Sign In|Join Free
  • or
5-Fluoro-2-methoxypyridine-3-boronic acid pinacol ester is a chemical compound characterized by the presence of a boronic acid group and a pinacol ester group. It is widely used in the field of organic synthesis, particularly for the creation of pharmaceuticals and agrochemicals. The boronic acid group enables participation in Suzuki-Miyaura coupling reactions, a prevalent method for forming carbon-carbon bonds in organic chemistry. The pinacol ester group enhances the stability and solubility of the compound, facilitating easier handling and storage. This versatile chemical is instrumental in the production of various essential substances in the pharmaceutical and agricultural industries.

1083168-95-9

Post Buying Request

1083168-95-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1083168-95-9 Usage

Uses

Used in Pharmaceutical Industry:
5-Fluoro-2-methoxypyridine-3-boronic acid pinacol ester is used as a reagent for the synthesis of various pharmaceuticals. Its boronic acid group allows it to participate in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds crucial for the development of new drugs. The pinacol ester group further enhances the compound's stability and solubility, making it easier to incorporate into pharmaceutical formulations.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Fluoro-2-methoxypyridine-3-boronic acid pinacol ester is employed as a reagent for the synthesis of agrochemicals. Its ability to participate in Suzuki-Miyaura coupling reactions facilitates the creation of carbon-carbon bonds necessary for the development of new agrochemicals. The pinacol ester group ensures the compound's stability and solubility, allowing for efficient incorporation into agrochemical formulations.
Used in Organic Synthesis:
5-Fluoro-2-methoxypyridine-3-boronic acid pinacol ester is used as a key intermediate in organic synthesis. Its boronic acid group allows it to participate in various cross-coupling reactions, enabling the formation of complex organic molecules. The pinacol ester group enhances the compound's stability and solubility, making it a valuable building block for the synthesis of a wide range of organic compounds.
Used in Research and Development:
In research and development, 5-Fluoro-2-methoxypyridine-3-boronic acid pinacol ester is utilized as a versatile reagent for exploring new chemical reactions and synthesizing novel compounds. Its ability to participate in Suzuki-Miyaura coupling reactions and other cross-coupling processes makes it an essential tool for chemists working on the development of new pharmaceuticals, agrochemicals, and other organic compounds.
Used in Academic and Industrial Laboratories:
5-Fluoro-2-methoxypyridine-3-boronic acid pinacol ester is employed as a reagent in academic and industrial laboratories for conducting experiments and research in the field of organic chemistry. Its unique properties, such as the boronic acid group and pinacol ester group, make it a valuable resource for studying various chemical reactions and synthesizing new compounds with potential applications in pharmaceuticals, agrochemicals, and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1083168-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,3,1,6 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1083168-95:
(9*1)+(8*0)+(7*8)+(6*3)+(5*1)+(4*6)+(3*8)+(2*9)+(1*5)=159
159 % 10 = 9
So 1083168-95-9 is a valid CAS Registry Number.

1083168-95-9SDS

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 5-Fluoro-2-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 5-fluoro-2-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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:1083168-95-9 SDS

1083168-95-9Downstream Products

1083168-95-9Relevant academic research and scientific papers

PYRAZOLOPYRIMIDINE DERIVATIVE AS SELECTIVE TRK INHIBITOR

-

Paragraph 0092; 0093, (2021/08/05)

The present invention discloses a compound of formula (II), a tautomer thereof or a pharmaceutically acceptable salt thereof, and relates to use thereof in preparing a medicament for treating solid tumor-related diseases.

PYRROLOPYRIMIDINES AS CFTR POTENTIATORS

-

Paragraph 0576; 0577, (2018/06/04)

The present invention relates to compounds of Formula I, wherein R1a, R1b, R2, R3, R4, W, Y, and Z are as described herein, and pharmaceutically acceptable salts thereof. The compounds are potentiator

MODULATORS OF CFTR

-

Page/Page column 105, (2009/01/20)

Compounds of the present invention, and pharmaceutically acceptable compositions thereof, are useful as modulators of ATP-Binding Cassette ("ABC") transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator ("CFTR"). The present invention also relates to methods of treating CFTR mediated diseases using compounds of the present invention.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1083168-95-9