Welcome to LookChem.com Sign In|Join Free

CAS

  • or
5-Fluoro-2-methoxyphenylboronic acid is an organic compound that serves as a crucial building block in various organic syntheses. It is characterized by its white to off-white powdery appearance and is known for its role as a reagent in Suzuki coupling reactions and copper-catalyzed arylation reactions. Additionally, it has been identified as a bacterial mutagen, highlighting its potential applications in research and development.

179897-94-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 179897-94-0 Structure
  • Basic information

    1. Product Name: 5-Fluoro-2-methoxyphenylboronic acid
    2. Synonyms: RARECHEM AH PB 0134;AKOS BRN-0214;5-FLUORO-2-METHOXYBENZENEBORONIC ACID;5-FLUORO-2-METHOXYPHENYLBORONIC ACID;3-FLUORO-6-METHOXYBENZENEBORONIC ACID;2-METHOXY-5-FLUOROBENZENEBORONIC ACID;2-METHOXY-5-FLUOROPHENYLBORONIC ACID;CHEMBRDG-BB 4202998
    3. CAS NO:179897-94-0
    4. Molecular Formula: C7H8BFO3
    5. Molecular Weight: 169.95
    6. EINECS: N/A
    7. Product Categories: blocks;BoronicAcids;FluoroCompounds;Substituted Boronic Acids;Boronic Acid;Alkoxy;Aryl;Organoborons;Boronic Acids;Boronic Acids and Derivatives;Aryl Boronic Acids;Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Disubstituted Aryl Boronic Acids;Organometallic Reagents;Furans
    8. Mol File: 179897-94-0.mol
  • Chemical Properties

    1. Melting Point: 144-153 °C(lit.)
    2. Boiling Point: 337.1 °C at 760 mmHg
    3. Flash Point: 157.6 °C
    4. Appearance: White/Crystalline Powder
    5. Density: 1.26 g/cm3
    6. Vapor Pressure: 2.08E-05mmHg at 25°C
    7. Refractive Index: 1.552
    8. Storage Temp.: N/A
    9. Solubility: soluble in Methanol
    10. PKA: 7.52±0.58(Predicted)
    11. CAS DataBase Reference: 5-Fluoro-2-methoxyphenylboronic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-Fluoro-2-methoxyphenylboronic acid(179897-94-0)
    13. EPA Substance Registry System: 5-Fluoro-2-methoxyphenylboronic acid(179897-94-0)
  • Safety Data

    1. Hazard Codes: Xi,Xn
    2. Statements: 36/37/38-20/21/22
    3. Safety Statements: 26-36/37/39-36-24/25
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 179897-94-0(Hazardous Substances Data)

179897-94-0 Usage

Uses

Used in Organic Synthesis:
5-Fluoro-2-methoxyphenylboronic acid is used as a key building block in organic synthesis for the creation of various complex molecules and compounds. Its unique structure allows for the formation of new chemical bonds and the synthesis of a wide range of organic molecules.
Used in Suzuki Coupling Reactions:
In the field of chemistry, 5-Fluoro-2-methoxyphenylboronic acid is utilized as a reagent for Suzuki coupling reactions. These reactions are essential for the formation of carbon-carbon bonds, which are vital in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
Used in Copper-Catalyzed Arylation Reactions:
5-Fluoro-2-methoxyphenylboronic acid also plays a significant role in copper-catalyzed arylation reactions. These reactions are crucial for the synthesis of aromatic compounds, which are widely used in the chemical, pharmaceutical, and materials industries.
Used in Research and Development:
As a bacterial mutagen, 5-Fluoro-2-methoxyphenylboronic acid is employed in research and development for studying the effects of mutations on bacterial cells. This application is essential for understanding the mechanisms of bacterial resistance and the development of new antibiotics and antimicrobial agents.

Check Digit Verification of cas no

The CAS Registry Mumber 179897-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,8,9 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179897-94:
(8*1)+(7*7)+(6*9)+(5*8)+(4*9)+(3*7)+(2*9)+(1*4)=230
230 % 10 = 0
So 179897-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BFO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9-11H

179897-94-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (F0775)  5-Fluoro-2-methoxyphenylboronic Acid (contains varying amounts of Anhydride)  

  • 179897-94-0

  • 5g

  • 390.00CNY

  • Detail
  • TCI America

  • (F0775)  5-Fluoro-2-methoxyphenylboronic Acid (contains varying amounts of Anhydride)  

  • 179897-94-0

  • 25g

  • 1,540.00CNY

  • Detail
  • Alfa Aesar

  • (H32748)  5-Fluoro-2-methoxybenzeneboronic acid, 98%   

  • 179897-94-0

  • 5g

  • 424.0CNY

  • Detail
  • Alfa Aesar

  • (H32748)  5-Fluoro-2-methoxybenzeneboronic acid, 98%   

  • 179897-94-0

  • 25g

  • 1623.0CNY

  • Detail

179897-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-fluoro-2-methoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 2-Methoxy-5-fluorophenylboronic 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:179897-94-0 SDS

179897-94-0Relevant articles and documents

HALOGENATED CATALYSTS COMPRISING SALAN LIGANDS

-

Page/Page column 47; 48, (2014/02/16)

Catalysts comprising a halogenated Salan ligand. Also disclosed are catalyst systems comprising the catalyst and an activator; methods to prepare the ligands, catalysts and catalyst systems; processes to polymerize olefins using the catalysts and/or catalyst systems; and the olefin polymers prepared according to the processes.

New series of morpholine and 1,4-oxazepane derivatives as dopamine D 4 receptor ligands: Synthesis and 3D-QSAR model

Audouze, Karine,Nielsen, Elsebet ?stergaard.,Peters, Dan

, p. 3089 - 3104 (2007/10/03)

Since the identification of the dopamine D43 receptor subtype and speculations about its possible involvement in schizophrenia, much work has been put into development of selective D4 ligands. These selective ligands may be effective antipsychotics without extrapyramidal side effects. This work describes the synthesis of a new series of 2,4-disubstituted morpholines and 2,4-disubstituted 1,4-oxazepanes with selectivity for the dopamine D4 receptor. A 3D-QSAR analysis using the GRID/GOLPE methodology was performed with the purpose to get a better understanding of the relationship between chemical structure and biological activity. Inspection of the coefficient plots allowed us to identify that regions which are important for affinity are situated around the two benzene ring systems, a p-chlorobenzyl group, and the aliphatic amine belonging to the morpholine or 1,4-oxazepane system. In addition, the size of the morpholine or 1,4-oxazepane ring seems to be important for affinity.

Substituted 3-amino biaryl propionic acids as potent VLA-4 antagonists.

Kopka, Ihor E,Lin, Linus S,Mumford, Richard A,Lanza Jr., Thomas,Magriotis, Plato A,Young, David,DeLaszlo, Stephen E,MacCoss, Malcolm,Mills, Sander G,Van Riper, Gail,McCauley, Ermengilda,Lyons, Kathryn,Vincent, Stella,Egger, Linda A,Kidambi, Usha,Stearns, Ralph,Colletti, Adria,Teffera, Yohannes,Tong, Sharon,Owens, Karen,Levorse, Dorothy,Schmidt, John A,Hagmann, William K

, p. 2415 - 2418 (2007/10/03)

A series of substituted N-(3,5-dichlorobenzenesulfonyl)-(L)-prolyl- and (L)-azetidyl-beta-biaryl beta-alanine derivatives was prepared as selective and potent VLA-4 antagonists. The 2,6-dioxygenated biaryl substitution pattern is important for optimizing potency. Oral bioavailability was variable and may be a result of binding to circulating plasma proteins.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

Steroid receptor modulator compounds and methods

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

Steroid receptor modulator compounds and methods

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiting steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

Tricyclic steroid receptor modulator compounds and methods

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

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 179897-94-0