JOHN J FOX
Vehicle Board in Baltimore, MD

License number
Pennsylvania MV132482L
Category
Vehicle Board
Type
Vehicle Salesperson
Address
Address 2
Baltimore, MD 21227
Pennsylvania

Personal information

See more information about JOHN J FOX at radaris.com
Name
Address
Phone
John Fox, age 62
508 S Bryn Mawr Ave, Bryn Mawr, PA 19010
(267) 252-1052
John Fox
5079 Hoppenville Rd, Green Lane, PA 18054
(215) 266-7045
John Fox, age 71
502 Wedgewood Ln, Canonsburg, PA 15317
(610) 866-4655
John Fox, age 83
525 Centennial St, Schwenksville, PA 19473
(610) 287-7342
John Fox
521 Cooper Dr, Warminster, PA 18974

Professional information

John Fox Photo 1

The Hut At Java

Position:
The Hut at Java
Location:
Baltimore, Maryland Area
Industry:
Nanotechnology
Work:
Java - The Hut


John Fox Photo 2

Owner, Rockland Credit

Position:
Owner at Rockland Credit
Location:
Baltimore, Maryland Area
Industry:
Financial Services
Work:
Rockland Credit - Owner
Education:
University of Cambridge


John Fox Photo 3

Attorney At Sellers, Fox, Kahn &Amp; Bender

Position:
Attorney at Sellers, Fox, Kahn & Bender
Location:
Baltimore, Maryland Area
Industry:
Law Practice
Work:
Sellers, Fox, Kahn & Bender - Attorney


John Fox Photo 4

Benzofuran Dyes Containing A Coumarin Nucleus

US Patent:
4973694, Nov 27, 1990
Filed:
Aug 17, 1989
Appl. No.:
7/394905
Inventors:
Chin H. Chen - Fairport NY
John L. Fox - Baltimore MD
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D491106, C07D40706
US Classification:
546 66
Abstract:
A 6-tertiary amino-2-(Z. dbd. CH--)benzofuran dye is disclosed, where Z represents the atoms providing an electron withdrawing group and a conjugated methine linkage completing a resonant dye chromophore including the 6-tertiary amino group as an electron donor and the electron withdrawing group as an electron acceptor. The dyes are formed by condensing a 6-tertiary amino-2-formylbenzofuran with an electron withdrawing dye nucleus precursor containing an active methyl or methylene site. The dyes exhibit bathocromically shifted absorption peaks.


John Fox Photo 5

Certain Intracyclic Or Extracyclic Phosphorous Containing Coumarins Useful As Laser Dyes

US Patent:
4727144, Feb 23, 1988
Filed:
Mar 31, 1986
Appl. No.:
6/846415
Inventors:
Chin H. Chen - Webster NY
John L. Fox - Baltimore MD
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07F 938, C07F 965
US Classification:
546 23
Abstract:
Phosphonocoumarins and phosphacoumarin lasing dyes are disclosed.


John Fox Photo 6

Novel Benzofuran Dyes

US Patent:
4948893, Aug 14, 1990
Filed:
Aug 17, 1989
Appl. No.:
7/394893
Inventors:
Chin H. Chen - Fairport NY
John L. Fox - Baltimore MD
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D49106
US Classification:
546 66
Abstract:
A 6-tertiary amino-2-(Z. dbd. CH--)benzofuran dye is disclosed, where Z represents the atoms providing an electron withdrawing group and a conjugated methine linkage completing a resonant dye chromophore including the 6-tertiary amino group as an electron donor and the electron withdrawing group as an electron acceptor. The dyes are formed by condensing a 6-tertiary amino-2-formylbenzofuran with an electron withdrawing dye nucleus precursor containing an active methyl or methylene site. The dyes exhibit bathochromically shifted absorption peaks.


John Fox Photo 7

Substituted Cyclopentadiene Electron Transport Compounds

US Patent:
5103038, Apr 7, 1992
Filed:
Nov 20, 1989
Appl. No.:
7/438813
Inventors:
Chin H. Chen - Fairport NY
John L. Fox - Baltimore MD
Yann Hung - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07C25531, C07C25550
US Classification:
558426
Abstract:
Novel tetrasubstituted dicyanomethylene cyclopentadienes are provided which have utility as electron-transport agents in positively-charged electrophotographic elements. The compounds are characterized by the formula: ##STR1## wherein: R. sub. 1 and R. sub. 4 are each independently selected from the group consisting of lower alkyl, halogen and cyano; R. sub. 2 and R. sub. 3 are each independently selected from the group consisting of aryl and substituted aryl; and Z and Z' are each an electron withdrawing group.


John Fox Photo 8

Benzopyrano[6,7,8-I,J]Quinolizine-11-One Lasing Dyes And Intermediates For Their Preparation

US Patent:
4736032, Apr 5, 1988
Filed:
Dec 30, 1985
Appl. No.:
6/814460
Inventors:
John L. Fox - Baltimore MD
Chin H. Chen - Webster NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D49106, C07D22106
US Classification:
546 66
Abstract:
Novel benzopyrano[6,7,8-i,j]quinolizine-11-one lasing dyes and intermediates for their preparation are disclosed.


John Fox Photo 9

Dye Sensitized Photographic Imaging Systems

US Patent:
4876175, Oct 24, 1989
Filed:
May 9, 1988
Appl. No.:
7/191947
Inventors:
Chin H. Chen - Fairport NY
John L. Fox - Baltimore MD
Donald P. Specht - Rochester NY
Samir Y. Farid - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 172
US Classification:
430281
Abstract:
A photographic imaging system is disclosed comprised of a hardenable organic component containing ethylenic unsaturation sites and coinitiators for ethylenic addition. The coinitiators include an activator and a photosensitizer. The photosensitizer is a 6-tertiary amino-2-(Z--CH. dbd. )benzofuran dye, where Z represents the atoms providing an electron withdrawing carbonyl or sulfonyl group and completing a conjugated methine linkage extending from the electron withdrawing carbonyl group through the benzofuran to the electron donating 6-tertiary amino substituent to form a resonant dye chromophore. The photosensitizers bathochromically extend exposure response of the imaging system.


John Fox Photo 10

Novel Benzofuran Dyes

US Patent:
4900831, Feb 13, 1990
Filed:
May 9, 1988
Appl. No.:
7/191948
Inventors:
Chin H. Chen - Fairport NY
John L. Fox - Baltimore MD
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D491147, C07D51900
US Classification:
546 66
Abstract:
A 6-tertiary amino-2-(Z. dbd. CH--)benzofuran dye is disclosed, where Z represents the atoms providing an electron withdrawing group and a conjugated methine linkage completing a resonant dye chromophore including the 6-tertiary amino group as an electron donor and the electron withdrawing group as an electron acceptor. The dyes are formed by condensing a 6-tertiary amino-2-formylbenzofuran with an electron withdrawing dye nucleus precursor containing an active methyl or methylene site. The dyes exhibit bathochromically shifted absorption peaks.