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Fabomotizole

  1. #1
    Cosmopolitan Tuskegee Airman
    https://en.m.wikipedia.org/wiki/Fabomotizole
  2. #2
    ner vegas Space Nigga
  3. #3
    the man who put it in my hood Black Hole [miraculously counterclaim my golf]
    I've never seen a drug so bad that the medical community refuses to write literature about it
  4. #4
    Speedy Parker Black Hole
    Originally posted by the man who put it in my hood I've never seen a drug so bad that the medical community refuses to write literature about it

    If they don't write about how would you know?
  5. #5
    Semiazas African Astronaut
    If a tree falls in the forest...
  6. #6
    Speedy Parker Black Hole
    Originally posted by Semiazas If a tree falls in the forest…

    And lands on a liberal does anyone care?
  7. #7
    Semiazas African Astronaut
    Originally posted by Speedy Parker And lands on a liberal does anyone care?

    If it's black, it's an excuse for a riot
    The following users say it would be alright if the author of this post didn't die in a fire!
  8. #8
    the man who put it in my hood Black Hole [miraculously counterclaim my golf]
    Originally posted by Speedy Parker If they don't write about how would you know?

    I think you answered your own question there sparky
  9. #9
    Speedy Parker Black Hole
    Originally posted by the man who put it in my hood I think you answered your own question there sparky

    You think a lot of other dumb shit too Timmy
  10. #10
    Instigator Naturally Camouflaged [the staring tame crusher]
    Originally posted by Cosmopolitan https://en.m.wikipedia.org/wiki/Fabomotizole

    Sounds fab.
  11. #11
    the man who put it in my hood Black Hole [miraculously counterclaim my golf]
    4-[2-[(6-ethoxy-1H-benzimidazol-2-yl)sulfanyl]ethyl]morpholine



    This class of drugs falls under the Benzimidazole class compounds as shown by the fused benzene ring
    https://en.wikipedia.org/wiki/Benzimidazole

    Benzimidazole was discovered during research on vitamin B12. The benzimidazole nucleus was found to be a stable platform on which drugs could be developed.[3] Benzimidazole is produced by condensation of o-phenylenediamine with formic acid,[4] or the equivalent trimethyl orthoformate:

    C6H4(NH2)2 + HC(OCH3)3 → C6H4N(NH)CH + 3 CH3OH

    2-Substituted derivatives are obtained when the condensation is conducted with aldehydes in place of formic acid, followed by oxidation.

    to produce FABOMOTIZOLE you would need to substitute 6-ethoxybenzimidazole using ethoxy-substituted o-phenylenediamine and an aldehyde. There should be a patent for this somewhere online
  12. #12
    Instigator Naturally Camouflaged [the staring tame crusher]
    Does it fuck me up though?
  13. #13
    the man who put it in my hood Black Hole [miraculously counterclaim my golf]
    Unlike benzodiazepines, Fabomotizole does not cause sedation, muscle relaxation, or dependency.
    Its effect is described as "mild anxiolysis," making it more of a calming agent for moderate anxiety rather than a potent tranquilizer.
    It has a slower onset of action compared to benzodiazepines but is considered safer for long-term use because of the lack of addiction potential.

    Don't know why anyone would make this junk on purpose unless you had a bunch of 6-ethoxybenzimidazole laying around. Seems like something only a broke bitch in eastern europe would make.

    You can mix it with Mercaptans to make a pretty yellow dye


    Making the dye would be way better because Mercaptans are a meme from how bad they smell and can also be used to make Novichok agents WAIT A SECOND
    The novichok reaction is the "Allen Reaction" between two moles of a trialkyl posphite and one molea beta-trihalonitroalkane, the most familiar such compound being trichloronitromethane, (chloropicrin) Cl3CNO2. The much less familiar nitroso compound Cl3CNO also works. There are some constraints on the choice of substituents.

    1. One of these must be chlorine, this is what attacks phosphorus initially.

    2. The others may be Cl, Br, F or a psuedohalogen e.g. -CN. These are the substituents that remain in the oxime ester side chain. These may be identical or different.

    The product is an exime ester of a dialkyl, dialkoxy, alkyl halo, or alkoxyhalophosphate.
    The preparation of the chloropicrin and analogs is well known.

    The most convenient prep of trichloronitrosomethane is one starting from trichloromethyl sulfenyl chloride, also known as perchloromethyl mercaptan, the familiar product of chlorination of CS2 with dry chlorine in diffuse light.

    This is oxidized to trichloromethylsulfonyl chloride according to the procedure of Prandl and coworker in Ber., 62 1752, (1929). A technical grade of this may be available from Eastman Kodak.

    The sulfonyl chloride is reduced with sodium in ethanol by the technique of Prandle and coworker in Ber. 65 (1932). The product is sodium trichloromethylsulffinate.

    The procedure described in same peper for preparing the trichloronitrosomethane, a deep blue liquid, from the sodium salt of the trichloromethylsulfinic acid is simple but causes some thermal decomposition and also produces a product not free from water.

    The same salt can be reacted in the cold with nitrosyl chloride in liquid phase, under autogenous pressure, the reaction being complete when the mixture is allowed to warm to O C. This procedure is detailed in a paper by Suttcliffe in JACS 79 3071 (1975). The anhydrous trichloromethylnitrosomethane is well suited for use directly in the Allen reaction.

    https://archive.org/details/DTIC_AD0052118
  14. #14
    the man who put it in my hood Black Hole [miraculously counterclaim my golf]
    building a dye factory next to a Fabomotizole factory would be a great way to hide a chemical weapons lab if you just ran a tunnel under them
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