What is Phenazepam Elzepam Bonsai Supersleep
Phenazepam is a 1,4-benzodiazepine, and is structurally similar to others in this class, including diazepam, oxazepam, and temazepam. The most significant structural difference is substitution of a bromine atom for chlorine in the 7 position of the phenyl ring.
It was developed in the former Soviet Union in 1975. Phenazepam is a benzodiazepine not currently controlled under the UN conventions, developed for treatment of epilepsy, alcohol withdrawal syndrome, insomnia and anxiety.
Currently prescribed only in Russia and some countries of the former Soviet Bloc, and first identified as an illicitly used substance in Europe in 2007.
The chemical name is 7‑bromo-5-(2-cholorphenyl)−1,3-dihydro-1,4-benzodiazepin-2-one. Phenazepam has a molecular weight 349.61 g/mol. It is also known as fenazepam, and with the street names “bonsai”, “bonsai supersleep”, and “soviet benzo”.
Phenazepam is generally encountered in either powder or tablet form, sometimes with the markings of legimitate benzodiazepines, such as diazepam, but also reported in spiked lysergic acid diethylamide blotters and a synthetic cannabinoid mix [5,23,24]. Forensic seizures have reported phenazepam identified as white powder or blue tablets.
Phenazepam (also known in Russia as bromdihydrochlorphenylbenzodiazepine) is a benzodiazepine drug, first developed in the Soviet Union in 1975, and now produced in Russia and several other countries.
Phenazepam is used in the treatment of various mental disorders such schizophrenia[citation needed] and anxiety. It can be used as a premedication before surgery as it augments the effects of anesthetics.
In 2009, phenazepam has gained popularity as a recreational drug; misuse has been reported in the United Kingdom, Finland, Sweden, and the United States.Phenazepam is a drug of the benzodiazepine class.
Benzodiazepine drugs contain a benzene ring fused to a diazepine ring, which is a seven membered ring with the two nitrogen constituents located at R1 and R4.
The benzyl ring of phenazepam is substituted at R7 with a bromine group. Like most benzodiazepines, phenazepam has a phenyl ring in R5 which is substituted by chlorine in the R2′ group.
Phenazepam also contains an oxygen group double bonded to R2 of its diazepine ring to form a ketone. This oxygen substitution at R2 is shared with other benzodiazepine drugs with the suffix -azepam.
Like other benzodiazepines, phenazepam (7-bromo-5-(2-chlorophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one) is composed of a benzene ring fused to a seven-membered 1,4-diazepine ring.
A 2-chlorophenyl ring is attached at the 5-position and a bromine is attached at the 7-position. Phenazepam has a molecular formula of C15H10BrClN2O and a molecular weight of 349.6 g/mol.
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