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Michael E O'Dea, 591 Broad St UNIT 30B, Stamford, CT 06901

Michael O'Dea Phones & Addresses

1 Broad St UNIT 30B, Stamford, CT 06901    860-5639198   

Wilton, CT   

Carmel, IN   

Middletown, CT   

Lafayette, IN   

Bridgeport, CT   

Frankfort, IN   

16 Glen Rdg, Wilton, CT 06897   

Social networks

Michael E O'Dea

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Education

School / High School: Mass Bay Community College

Mentions for Michael E O'Dea

Career records & work history

Lawyers & Attorneys

Michael O'Dea Photo 1

Michael O'Dea - Lawyer

ISLN:
922074509
Admitted:
2008
Michael O'Dea Photo 2

Michael O'Dea - Lawyer

ISLN:
1001172340
Admitted:
2021

Michael O'Dea resumes & CV records

Resumes

Michael O'Dea Photo 27

Michael O'dea

Education:
Mass Bay Community College

Publications & IP owners

Us Patents

Loracarbef Isopropanolate

US Patent:
5672700, Sep 30, 1997
Filed:
Dec 1, 1994
Appl. No.:
8/347759
Inventors:
William C. Henning - Lafayette IN
Michael E. O'Dea - Lafayette IN
Assignee:
Eli Lilly and Company - Indianapolis IN
International Classification:
C07D48704
A61K 31435
US Classification:
540205
Abstract:
The invention is directed to the crystalline isopropyl alcohol solvate of loracarbef, and also is directed to a process for the preparation of the crystalline monohydrate form of the compound of formula (I) ##STR1## which includes exposing the crystalline isopropyl solvate form of the compound of formula (I) to a temperature of between about 50. degree. and 90. degree. C. and a relative humidity of between about 60 to about 100%.

Loracarbef Isopropanolate And A Process For Converting Loracarbef Isopropanolate To Loracarbef Monohydrate

US Patent:
5399686, Mar 21, 1995
Filed:
Jun 4, 1993
Appl. No.:
8/072204
Inventors:
William C. Henning - Lafayette IN
Michael E. O'Dea - Lafayette IN
Assignee:
Eli Lilly and Company - Indianapolis IN
International Classification:
C07D48704
A61K 31435
US Classification:
540205
Abstract:
The invention is directed to the crystalline isopropyl alcohol solvate of loracarbef, and also is directed to a process for the preparation of the crystalline monohydrate form of the compound of formula (I) ##STR1## which includes exposing the crystalline isopropyl solvate form of the compound of formula (I) to a temperature of between about 50. degree. and 90. degree. C. and a relative humidity of between about 60 to about 100%.

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