2,6-Difluorobenzeneboronic Acid (contains varying amounts of Anhydride) - ≥98% , CAS No.162101-25-9

CAS: 162101-25-9 Cat. No.: D100721 Molecular Weight: 157.91 EC Number: 627-874-1

GRADE & PURITY ≥98%

Synonyms

AKOS000285072 | D3087 | DTXSID70370227 | J-507481 | 2,6 difluorophenyl boronic acid | SCHEMBL146988 | 2,6-Difluorophenylboronicacid | 2,6-difluoro phenylboric acid | 2,6-Difluorophenylboronic acid, 98% | (2,6-difluorophenyl)boronic Acid | (2,6-difluorophe

Storage

Room temperature

Shipped In

Normal

Overview

Product Application

2,6-Difluorophenylboronic acid can be used:

1.As a substrate in the model reaction of Suzuki–Miyaura coupling with 4-chloro-3-methylanisole.

2.To prepare 4-bromo-2,3′,5′,6-tetrafluorobiphenyl, a key intermediate for the synthesis of 2,6-difluorinated oligophenyls applicable in organic semiconductors.

3.To prepare ethyl 4-(2,6-difluorophenyl)nicotinate, a key intermediate for the synthesis of 4-phenyl pyridine based potent TGR5 agonists.

Specifications

Synonyms

AKOS000285072 | D3087 | DTXSID70370227 | J-507481 | 2, 6 difluorophenyl boronic acid | SCHEMBL146988 | 2, 6-Difluorophenylboronicacid | 2, 6-difluoro phenylboric acid | 2, 6-Difluorophenylboronic acid, 98% | (2, 6-difluorophenyl)boronic Acid | (2, 6-difluorophe

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488192544
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488192544
• Canonical Smiles: B(C1=C(C=CC=C1F)F)(O)O
• IUPAC Name: (2,6-difluorophenyl)boronic acid
• InChIKey: DBZAICSEFBVFHL-UHFFFAOYSA-N
• INCHI: 1S/C6H5BF2O2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3,10-11H
• Isomeric SMILES: B(C1=C(C=CC=C1F)F)(O)O
• WGK Germany: 3
• Molecular Weight: 157.91
• Reaxy-Rn: 8545931
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8545931&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Halobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Halobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorobenzenes
• Alternative Parents: Aryl fluorides Boronic acids Organic metalloid salts Organofluorides Organoboron compounds Organic oxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Fluorobenzene - Aryl halide - Aryl fluoride - Boronic acid - Boronic acid derivative - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organofluoride - Organoboron compound - Organohalogen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as fluorobenzenes. These are compounds containing one or more fluorine atoms attached to a benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in Methanol
• Melt Point(°C): 147-149°C
• Molecular Weight: 157.910 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 158.035 Da
• Monoisotopic Mass: 158.035 Da
• Topological Polar Surface Area: 40.500 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 124.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

XLogP3