The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
May. 27, 1997

Filed:

Jul. 10, 1996
Applicant:
Inventors:

Ravi B Shankar, Midland, MI (US);

R Garth Pews, Midland, MI (US);

Duane R Romer, Midland, MI (US);

Assignee:

The Dow Chemical Company, Midland, MI (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A01N / ; A61K / ; C07D / ;
U.S. Cl.
CPC ...
504261 ; 514362 ; 548126 ;
Abstract

Various 5H-pyrrolo(3',4':5,6)(1,4) dithiino-(2,3-C)(1,2,5)thiadiazole-5,7(6H)-diones corresponding to the formula ##STR1## wherein R represents --H, benzyl, phenethyl, a C.sub.1 -C.sub.10 straight or branched chain alkyl radical, a C.sub.3 -C.sub.10 cycloalkyl radical, a C.sub.1 -C.sub.10 straight or branched chain alkoxy radical, a C.sub.3 -C.sub.10 -cycloalkoxy, an ester of the formula --CH.sub.2 CH.sub.2 O--C(O)--R.sup.1, wherein R.sup.1 represents a C.sub.1 -C.sub.6 straight or branched chain alkyl radical or a C.sub.3 -C.sub.6 cycloalkyl radical or R represents phenyl substituted with from 0-5 halo, C.sub.1 -C.sub.6 straight or branched chain alkyl, cyano, nitro groups, or an ester of the formula --OC(O)--R.sup.1, wherein R.sup.1 represents a C.sub.1 -C.sub.6 straight or branched chain alkyl radical or a C.sub.3 -C.sub.6 cycloalkyl radical or an amide of the formula --C(O)--N(R.sup.2).sub.x, wherein each R.sup.2 independently represents a C.sub.1 -C.sub.6 straight or branched chain alkyl radical or a C.sub.3 -C.sub.6 cycloalkyl radical are disclosed. These compounds have been found to exhibit antimicrobial and marine antifouling activity in industrial and commercial applications and compositions containing these compounds are so employed.


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