Home Other Building Blocks 1-Fluoronaphthalene

1-Fluoronaphthalene

CAS No.:
321-38-0
Catalog Number:
AG0032RJ
Molecular Formula:
C10H7F
Molecular Weight:
146.1610
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$50
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG0032RJ
Chemical Name:
1-Fluoronaphthalene
CAS Number:
321-38-0
Molecular Formula:
C10H7F
Molecular Weight:
146.1610
MDL Number:
MFCD00003873
IUPAC Name:
1-fluoronaphthalene
InChI:
InChI=1S/C10H7F/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H
InChI Key:
CWLKTJOTWITYSI-UHFFFAOYSA-N
SMILES:
Fc1cccc2c1cccc2
EC Number:
206-287-0
UNII:
0920702UT7
NSC Number:
4690
UN Number:
2810
Properties
Complexity:
133  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
146.053g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
146.164g/mol
Monoisotopic Mass:
146.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.7  
Literature
Title Journal
Density functional theory study of vibrational spectra, and assignment of fundamental vibrational modes of 1-bromo 4-fluoronaphthalene. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20081001
Design and synthesis of 6-fluoro-2-naphthyl derivatives as novel CCR3 antagonists with reduced CYP2D6 inhibition. Bioorganic & medicinal chemistry 20080915
N,N-Dimethyl-3-(1-naphth-yloxy)-3-(2-thien-yl)propan-1-amine. Acta crystallographica. Section E, Structure reports online 20080301
Characterization of monofluorinated polycyclic aromatic compounds by 1H, 13C and 19F NMR spectroscopy. Magnetic resonance in chemistry : MRC 20050701
Synthesis of highly oxygenated dinaphthyl ethers via SNAr reactions promoted by Barton's base. Organic letters 20030403
A one-pot access to 6-substituted phenanthridines from fluoroarenes and nitriles via 1,2-arynes. Organic letters 20020808
Properties