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Short description: Chemical compound
Clocental |
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| Other names | Dolcental |
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| Identifiers |
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(1-Ethynylcyclohexyl) N-carbamoylcarbamate
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| Chemical and physical data |
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| Formula | C10H14N2O3 |
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| Molar mass | 210.233 g·mol−1 |
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| 3D model (JSmol) | |
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C#CC1(CCCCC1)OC(=O)NC(=O)N
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InChI=1S/C10H14N2O3/c1-2-10(6-4-3-5-7-10)15-9(14)12-8(11)13/h1H,3-7H2,(H3,11,12,13,14)  YKey:CQVLNDZXTPGTFD-UHFFFAOYSA-N Y
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Clocental (dolcental) is a carbamate-derived sedative hypnotic. It can be prepared by the ethynylation of cyclohexanone followed by reaction with allophanyl chloride.[1]
See also
References
- ↑ Grimme W, Emde H, "Verfahren zur Herstellung von Allophanaten von α-Äthinylcarbinolen [Process for the preparation of allophanates of α-ethynyl carbinols]", DE patent 959458, issued 7 March 1957, assigned to Rheinpreußen AG fuer Bergbau und Chemie
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| Alcohols | |
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| Nonbenzodiazepines | |
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| Volatiles/gases | |
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| Others/unsorted |
- 3-Hydroxybutanal
- α-EMTBL
- AA-29504
- Avermectins (e.g., ivermectin)
- Bromide compounds (e.g., lithium bromide, potassium bromide, sodium bromide)
- Carbamazepine
- Chloralose
- Chlormezanone
- Clomethiazole
- DEABL
- Dihydroergolines (e.g., dihydroergocryptine, dihydroergosine, dihydroergotamine, ergoloid (dihydroergotoxine))
- DS2
- Efavirenz
- Etazepine
- Etifoxine
- Fenamates (e.g., flufenamic acid, mefenamic acid, niflumic acid, tolfenamic acid)
- Fluoxetine
- Flupirtine
- Hopantenic acid
- Lanthanum
- Lavender oil
- Lignans (e.g., 4-O-methylhonokiol, honokiol, magnolol, obovatol)
- Loreclezole
- Menthyl isovalerate (validolum)
- Monastrol
- Niacin
- Nicotinamide (niacinamide)
- Org 25,435
- Phenytoin
- Propanidid
- Retigabine (ezogabine)
- Safranal
- Seproxetine
- Stiripentol
- Sulfonylalkanes (e.g., sulfonmethane (sulfonal), tetronal, trional)
- Terpenoids (e.g., borneol)
- Topiramate
- Valerian constituents (e.g., isovaleric acid, isovaleramide, valerenic acid, valerenol)
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 | Original source: https://en.wikipedia.org/wiki/Clocental. Read more |
