38134-31-5 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(1-hydroxycyclopentyl)propan-2-one is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Drug Development:
1-(1-hydroxycyclopentyl)propan-2-one is also utilized in the development of new drugs, thanks to its potential to be modified and incorporated into various drug candidates. Its properties make it a promising starting point for the design of novel therapeutic agents.
Used in Drug Delivery Systems:
1-(1-hydroxycyclopentyl)propan-2-one may be employed as a component in the design of drug delivery systems, potentially enhancing the bioavailability and targeting of pharmaceuticals.
Used in Organic Chemistry:
As a ketone with a cyclopentyl group and a hydroxyl group, 1-(1-hydroxycyclopentyl)propan-2-one is a valuable building block in organic chemistry, allowing for the synthesis of a variety of complex organic molecules.
Safety Note:
It is important to handle 1-(1-hydroxycyclopentyl)propan-2-one with care, as it may possess toxic or hazardous properties. Proper safety measures should be taken during its use in research and development settings.
Check Digit Verification of cas no
The CAS Registry Mumber 38134-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,3 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38134-31:
(7*3)+(6*8)+(5*1)+(4*3)+(3*4)+(2*3)+(1*1)=105
105 % 10 = 5
So 38134-31-5 is a valid CAS Registry Number.
38134-31-5Relevant academic research and scientific papers
Cyclic Ether Synthesis via Palladium-Catalyzed Directed Dehydrogenative Annulation at Unactivated Terminal Positions
Thompson, Samuel J.,Thach, Danny Q.,Dong, Guangbin
supporting information, p. 11586 - 11589 (2015/09/28)
Here, a palladium-catalyzed functionalization of unactivated sp3 C-H bonds with internal alcohol nucleophiles is described. Directed by an oxime-masked alcohol, annulation chemoselectively occurs at the β position, leading to a range of aliphatic cyclic ethers with four- to seven-membered rings. Tethered primary, secondary, and tertiary free hydroxyl groups can all react to give the corresponding cyclized products. In addition, benzyl and silyl protected alcohols can also be directly coupled. An sp3 C-H activation/intramolecular SN2 pathway was proposed.
Chemistry of free cyclic vicinal tricarbonyl compounds ('1,2,3-triones'). Part 1. Reaction of diazomethane and its derivatives with 5,5-dimethylcyclohexane-1,2,3-trione (='oxo-dimedone') and related cyclohexane-1,2,3-triones
Schank, Kurt,La Vecchia, Luigi,Lick, Carlo
, p. 2071 - 2088 (2007/10/03)
Interactions of diazomethane and of its derivatives as typical nucleophiles with cyclic 1,2,3-triones as efficient electrophiles lead to different results: a) formation of oxiranes (C,O insertion under loss of N2), b) nucleophilic addition yiel
