Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2,6-Difluoropyridine-4-boronic acid is a chemical compound with the formula C5H4BF2NO2. It is a boronic acid derivative characterized by the presence of two fluorine atoms at the 2nd and 6th positions of the pyridine ring and a boronic acid group at the 4th position. 2,6-Difluoropyridine-4-boronic acid is widely used in organic synthesis and medicinal chemistry as a key building block for constructing various bioactive molecules and pharmaceuticals.

401816-16-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 401816-16-8 Structure
  • Basic information

    1. Product Name: 2,6-Difluoropyridine-4-boronic acid
    2. Synonyms: 2,6-DIFLUORO-4-PYRIDYLBORONIC ACID;(2,6-DIFLUOROPYRIDIN-4-YL)BORONIC ACID;2,6-DIFLUOROPYRIDINE-4-BORONIC ACID;Boronic acid, (2,6-difluoro-4-pyridinyl)- (9CI);B-(2,6-difluoro-4-pyridinyl)-Boronic acid;B-(2,6-Difluoro-pyridin-4-yl)boronic acid
    3. CAS NO:401816-16-8
    4. Molecular Formula: C5H4BF2NO2
    5. Molecular Weight: 158.9
    6. EINECS: N/A
    7. Product Categories: HALIDE;BORONICACID;Boronic acid;Organoborons;Pyridine;Pyridines
    8. Mol File: 401816-16-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 334 °C at 760 mmHg
    3. Flash Point: 155.8 °C
    4. Appearance: /
    5. Density: 1.44g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
    8. Solubility: N/A
    9. PKA: 5.46±0.11(Predicted)
    10. CAS DataBase Reference: 2,6-Difluoropyridine-4-boronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,6-Difluoropyridine-4-boronic acid(401816-16-8)
    12. EPA Substance Registry System: 2,6-Difluoropyridine-4-boronic acid(401816-16-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 37/38-41
    3. Safety Statements: 26-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 401816-16-8(Hazardous Substances Data)

401816-16-8 Usage

Uses

Used in Organic Synthesis:
2,6-Difluoropyridine-4-boronic acid is used as a reagent in the Suzuki-Miyaura cross-coupling reaction, a widely employed method for forming carbon-carbon bonds. Its versatile reactivity and functional group compatibility make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,6-Difluoropyridine-4-boronic acid serves as a key intermediate for the development of new drugs. Its unique structure and reactivity allow for the creation of novel bioactive compounds with potential therapeutic applications.
Used in Drug Development:
2,6-Difluoropyridine-4-boronic acid has potential applications in the development of new drugs and agrochemicals. Its ability to form stable carbon-carbon bonds and its compatibility with various functional groups make it a promising candidate for the synthesis of innovative pharmaceuticals and agrochemicals with improved efficacy and selectivity.
Used in the Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-Difluoropyridine-4-boronic acid is used as a building block for the synthesis of various bioactive molecules. Its unique structure and reactivity enable the development of new drugs with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used in the Agrochemical Industry:
In the agrochemical industry, 2,6-Difluoropyridine-4-boronic acid is utilized for the development of new agrochemicals, such as pesticides and herbicides. Its versatile reactivity and functional group compatibility contribute to the creation of novel compounds with enhanced performance and selectivity, leading to more effective and environmentally friendly agricultural solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 401816-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,8,1 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 401816-16:
(8*4)+(7*0)+(6*1)+(5*8)+(4*1)+(3*6)+(2*1)+(1*6)=108
108 % 10 = 8
So 401816-16-8 is a valid CAS Registry Number.

401816-16-8SDS

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 2,6-Difluoropyridine-4-boronic acid

1.2 Other means of identification

Product number -
Other names (2,6-difluoropyridin-4-yl)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:401816-16-8 SDS

401816-16-8Relevant articles and documents

Substituted pyridines

-

Page/Page column 5, (2008/06/13)

A class of 2,4-; 2,3,4-; 2,4,6-; 2,3,4,5,6-substituted pyridines is provided which include novel compounds. The substitutions are achieved according to methods disclosed herein in which a metallated pyridine is reacted with an electrophile. Suitable electrophiles include CO2, SO2, dialkylcarbonates, ureas, formamides, amides, carboxylic acid esters, mono- and dihaloalkyls, halogens such as chlorine, fluorine, bromine, and iodine, metallic salts, sulfones, sulfonyls, aldehydes, ketones, anhydrides, nitrites, and electrophilic boron compounds including, but not limited to, boron trialkoxides and boron trihalides. The subject invention more specifically discloses a process for the synthesis of 2,6-difluoropyridin-4-ylboronic acid which comprises: (1) reacting 2,4,6-trifluoropyridine with hydrazine monohydrate to produce 2,6-difluoro-4-hydrazinopyridine, (2) reacting the 2,6-difluoro-4-hydrazinopyridine with elemental bromine to produce 4-bromo-2,6-difluoropyridine, and (3) reacting the 4-bromo-2,6-difluoropyridine with an organolithium compound and a borate at a temperature of less than about 0° C. to produce the 2,6-difluoropyridin-4-ylboronic acid, wherein said process is conducted in an organic solvent.

Heterocyclic derivatives

-

, (2008/06/13)

The invention relates to heterocyclic derivatives of the formula I wherein R1, A1, Z1, n, A2, Z2, Q1, Q2, Q3 and L have the meaning given in claim 1 and to their use as components of liquid crystalline media for electro-optical displays.

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

What can I do for you?
Get Best Price

Get Best Price for 401816-16-8