Welcome to LookChem.com Sign In|Join Free
  • or
8-Fluoroquinoline-6-boronic acid is a chemical compound derived from the parent compound quinoline, featuring a fluoro substituent at the 8-position and a boronic acid group at the 6-position. It belongs to the quinolines group and is characterized by its boronic acid functional group, which makes it a versatile building block in organic synthesis and medicinal chemistry for the preparation of pharmaceuticals and biologically active molecules.

1210048-29-5

Post Buying Request

1210048-29-5 Suppliers

Recommended suppliers

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

1210048-29-5 Usage

Uses

Used in Organic Synthesis:
8-Fluoroquinoline-6-boronic acid is used as a building block for the synthesis of various organic compounds due to its ability to form covalent bonds with other molecules, particularly in cross-coupling reactions.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 8-Fluoroquinoline-6-boronic acid is used as a key intermediate in the development of new drugs and biologically active molecules. Its boronic acid moiety facilitates the formation of new chemical entities with potential therapeutic applications.
Used in Cross-Coupling Reactions:
8-Fluoroquinoline-6-boronic acid is employed as a reagent in cross-coupling reactions, which are essential for the synthesis of complex organic molecules and the modification of existing compounds to enhance their properties.
Used in Suzuki-Miyaura Coupling Reactions:
8-Fluoroquinoline-6-boronic acid is utilized in Suzuki-Miyaura coupling reactions, a type of cross-coupling reaction that allows for the formation of carbon-carbon bonds, enabling the synthesis of a wide range of organic compounds with potential applications in various fields, including pharmaceuticals and materials science.
Used in Drug Discovery and Development:
8-Fluoroquinoline-6-boronic acid is used as a tool in drug discovery and development due to the specific properties and interactions imparted by the fluoro substituent in biological systems, making it an important component in the design and synthesis of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1210048-29-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,0,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1210048-29:
(9*1)+(8*2)+(7*1)+(6*0)+(5*0)+(4*4)+(3*8)+(2*2)+(1*9)=85
85 % 10 = 5
So 1210048-29-5 is a valid CAS Registry Number.

1210048-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (8-Fluoroquinolin-6-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 8-fluoroquinolin-6-ylboric 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:1210048-29-5 SDS

1210048-29-5Relevant academic research and scientific papers

SUBSTITUTED 5-AMINOPYRAZOLES AND USE THEREOF

-

Page/Page column 132-133, (2010/04/03)

The present application relates to novel substituted 5-aminopyrazoles, methods of production thereof, use thereof alone or in combinations for the treatment and/or prophylaxis of diseases and use thereof for the production of medicinal products for the treatment and/or prophylaxis of diseases.

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 1210048-29-5