Clocental

In today's world, Clocental has become a relevant topic that attracts the attention of millions of people around the world. Since its appearance, Clocental has generated a significant impact in different areas, from politics to popular culture. Over the years, Clocental has sparked passionate debates and brought about major changes in the way people perceive the world around them. In this article, we will explore the evolution of Clocental over time and examine its influence on contemporary society.
Not to be confused with Placental.

Clocental
Structural formula
Ball-and-stick model of the clocental molecule
Clinical data
Other namesDolcental
Identifiers
  • (1-Ethynylcyclohexyl) N-carbamoylcarbamate
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC10H14N2O3
Molar mass210.233 g·mol−1
3D model (JSmol)
  • C#CC1(CCCCC1)OC(=O)NC(=O)N
  • 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) checkY
  • Key:CQVLNDZXTPGTFD-UHFFFAOYSA-N checkY

Clocental (dolcental) is a carbamate-derived sedative hypnotic.[1][2]

Synthesis

Clocental was first prepared by the acylation of 1-ethynylcyclohexanol with allophanyl chloride.[3]

See also

References

  1. ^ Keil W, Muschaweck R, Rademacher E (August 1954). "". Arzneimittel-Forschung (in German). 4 (8): 477–479. PMID 13198744.
  2. ^ Preuss R, Kopp R (April 1959). "". Arzneimittel-Forschung (in German). 9 (4): 255–262. PMID 13651050.
  3. ^ US patent 2822379, Grimme W, Emde H, "Allophanates of alpha-ethynylcarbinols", issued 1958-02-04, assigned to Rheinpreussen AG fuer Bergbau und Chemie 
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