Esters with antimicrobial, bioresistant and fungal resistant...

Organic compounds -- part of the class 532-570 series – Organic compounds – Nitriles

Reexamination Certificate

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C558S442000, C560S156000, C560S158000, C424S063000

Reexamination Certificate

active

11209377

ABSTRACT:
A bromine
itro moiety linked into the backbone of an ester or other compound over a wide range of occurrence rates provides antimicrobial, bio-resistant and fungal resistant properties for metal working fluids (MWF)s, coatings, plastics, and medical devices. The moiety can be have the bromo and nitro groups linked to the same or different carbon atoms. The present invention also relates to urethanes, urea, amides, imides, carbonates, ethers, siloxanes, and many other types of linkages essential to MWF bases.

REFERENCES:
patent: 5109020 (1992-04-01), Negele et al.
patent: 2000053502 (2000-02-01), None
Mdoe et al. Catalysis of the Michael reactions by N, N′-dimethylaminopropyl derivatised micelle templated silica: effects of solvent and loading. Bulletin of the Chemical Society of Ethiopia, 2003, vol. 17 (2), p. 219-233, ACS document No. 141:71146.
Park et al. Viologen-mediated reductive transformations of gem-bromonitro compounds and alpha-nitroketones by sodium dithionite. Bulletin of the Korean Chemical Society, 1993, vol. 14 (4) p. 461-465, ACS documents No. 120:133483.
Takeuchi et al. The First General and Efficient Method for the Synthesis of Tetriary Alkyl Fluorides. Journal of Organic Chemistry, 1993, vol. 58 (13) p. 3483-3485.
Piquet et al. Michael Additions of Carbonucleophiles to Butenone Catalyzed by the Non-Hydride [Ru(O2CH)(CO)2(PPh3)]2 Complex. Tetrahedron, 1999, vol. 55 (13) p. 3937-3948.
Klemm et al. Thin-layer chromatagraphic studies on derivatives of the biocide 2-bromo-2-nitropropane. Journal of Chromatagraphy, 1988, vol. 438 (1), p. 122-125. See ACS doc. No. 109:21609.

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