Home Boronic acids 4-Fluorophenylboronic acid

4-Fluorophenylboronic acid

CAS No.:
1765-93-1
Catalog Number:
AG0024PV
Molecular Formula:
C6H6BFO2
Molecular Weight:
139.9200
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
10g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$24
- +
100g
98%
In Stock USA
United States
$63
- +
500g
98%
In Stock USA
United States
$244
- +
Product Description
Catalog Number:
AG0024PV
Chemical Name:
4-Fluorophenylboronic acid
CAS Number:
1765-93-1
Molecular Formula:
C6H6BFO2
Molecular Weight:
139.9200
MDL Number:
MFCD00039136
IUPAC Name:
(4-fluorophenyl)boronic acid
InChI:
InChI=1S/C6H6BFO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI Key:
LBUNNMJLXWQQBY-UHFFFAOYSA-N
SMILES:
OB(c1ccc(cc1)F)O
NSC Number:
142683
Properties
Complexity:
102  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
140.044g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
139.92g/mol
Monoisotopic Mass:
140.044g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
1,8-Bis(4-fluoro-phen-yl)naphthalene. Acta crystallographica. Section E, Structure reports online 20110701
Phenylboronic-acid-based carbohydrate binders as antiviral therapeutics: monophenylboronic acids. Antiviral chemistry & chemotherapy 20100811
Aryl boronic acid inhibition of synthetic melanin polymerization. Bioorganic & medicinal chemistry letters 20100801
Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase. Journal of medicinal chemistry 20081127
Synthesis and biological evaluation of NAS-21 and NAS-91 analogues as potential inhibitors of the mycobacterial FAS-II dehydratase enzyme Rv0636. Microbiology (Reading, England) 20080701
2,4,6-Tris-(4-fluoro-phen-yl)-2-(1-pyrid-yl)-boroxine. Acta crystallographica. Section E, Structure reports online 20080101
An antifungal agent inhibits an aminoacyl-tRNA synthetase by trapping tRNA in the editing site. Science (New York, N.Y.) 20070622
Properties