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Cyrax (Hive Bee) 06-06-02 00:09 No 317965 |
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methoxyacetyl chloride | Bookmark | |||||
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Is it suspicious to buy methoxyacetyl chloride? Is it a watched chemical? |
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Rhodium (Chief Bee) 06-06-02 00:36 No 317972 |
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I'd say that is obscure enough to be safe. | Bookmark | |||||
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I'd say that is obscure enough to be safe. |
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PrimoPyro (Hive Prodigy) 06-06-02 02:49 No 318046 |
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Curious | Bookmark | |||||
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Methoxyacetyl chloride... CH3-O-CH2-CO-Cl correct? What use would this have clandestinely? Just curious. PrimoPyro |
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Cyrax (Hive Bee) 06-06-02 13:39 No 318206 |
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Well, you can use it instead of propionyl ... | Bookmark | |||||
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Well, you can use it instead of propionyl chloride or propionic anhydride to acylate 1-phenethyl-4-(N-phenylamino)-piperidine Or you can use 2-furoyl chloride to the amine. That compound will certainly not be suspicious. Then the ED50 is 0.02 mg / kg. |
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Rhodium (Chief Bee) 06-06-02 13:44 No 318208 |
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Fentanalogs | Bookmark | |||||
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Cyrax: Very interesting! Refs? |
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Nemo_Tenetur (Newbee) 06-06-02 13:45 No 318209 |
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... and bypass some analogue laws ! | Bookmark | |||||
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Very good idea! Although somewhat weaker, you can get around U.K. generic definition (and maybe same in some other countries) |
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Cyrax (Hive Bee) 06-06-02 18:17 No 318274 |
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Check it out: US patent 4584303. (Rated as: excellent) |
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Check it out: US patent 4584303. You will find a real treasure of fentanyl analogs. It is one of the best fentanyl patents I have read. Too weak: I think it is strong enough to not kill yourself during the synthesis. If you want a stronger compound: simply use o-fluoroaniline instead of aniline. Then the ED50 will be 0.0077 mg / kg. But I forsee that the yield of the acylation will be lower, since that lovely little fluorine atom will suck the free electron pair of the nitrogen into the aryl ring |
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