| 词条 | Clocental |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = (1-Ethynylcyclohexyl) N-carbamoylcarbamate | synonyms = Dolcental | image = Dolcental.png | alt = Structural formula | image2 = Clocental molecule ball.png | alt2 = Ball-and-stick model of the clocental molecule | width = 200 | tradename = | pregnancy_category = | legal_status = | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 562-94-7 | ATC_prefix = | ATC_suffix = | PubChem = | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 10757 | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = | KEGG_Ref = {{keggcite|changed|kegg}} | KEGG = | C=10 | H=14 | N=2 | O=3 | molecular_weight = 210.22976 g/mol | smiles = C#CC1(CCCCC1)OC(=O)NC(=O)N | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 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) | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = CQVLNDZXTPGTFD-UHFFFAOYSA-N }}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
References1. ^Grimme, Walter; Emde, Hans {{Cite patent|DE|959458}} (1957 to Rheinpreussen) {{Hypnotics and sedatives}}{{GABAAR PAMs}} 5 : Alkynes|Carbamates|Hypnotics|Sedatives|GABAA receptor positive allosteric modulators |
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