14675-44-6 Usage
Uses
Used in Pharmaceutical Industry:
(1,4-DIMETHYL-2-PIPERAZINYL)METHANOL is used as a pharmaceutical intermediate for the synthesis of various medications, including antipsychotics, antihistamines, and antimalarial drugs. Its unique chemical structure allows it to be a key component in the development of these therapeutic agents.
Used in Chemical Industry:
(1,4-DIMETHYL-2-PIPERAZINYL)METHANOL is used as a corrosion inhibitor, helping to protect metal surfaces from degradation and extending their service life. Its ability to form complexes with metal ions makes it an effective agent in preventing corrosion.
(1,4-DIMETHYL-2-PIPERAZINYL)METHANOL is also used as a polymerization catalyst, facilitating the process of polymer formation and improving the efficiency of the reaction. Its catalytic properties contribute to the production of various polymers used in different industries.
Furthermore, (1,4-DIMETHYL-2-PIPERAZINYL)METHANOL serves as a precursor to other organic compounds, enabling the synthesis of a diverse range of chemical products. Its role in the formation of these compounds highlights its importance in the chemical industry.
It is crucial to handle and use (1,4-DIMETHYL-2-PIPERAZINYL)METHANOL with caution, as it can be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken to minimize potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 14675-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14675-44:
(7*1)+(6*4)+(5*6)+(4*7)+(3*5)+(2*4)+(1*4)=116
116 % 10 = 6
So 14675-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-8-3-4-9(2)7(5-8)6-10/h7,10H,3-6H2,1-2H3
14675-44-6Relevant academic research and scientific papers
Interaction of (α-Haloalkyl)thiiranes with Nucleophilic Reagents. II. Reaction of (α-Chloroalkyl)thiiranes and Epihalohydrins with N,N′-Dimethylethylenediamine
Tomashevskii,Sokolov,Potekhin
, p. 583 - 588 (2007/10/03)
The (chloromethyl)thiirane reacts with N,N′-dimethylethylenediamine at heating in toluene to yield a mixture of 1,4-dimethylpiperazine-2-methanethiol and hexahydro-1,4-dimethyl-1,4-diazepine-6-thiol in 2: 1 ratio. The 2-methyl-2-(chloromethyl)thiirane under similar condition forms only the respective diazepine homolog in a low yield, while the diastereomers eritro- and threo-(1-chloroethyl)thiirans react stereospecifically to afford the corresponding eritro- and threo-α,1,4-trimethylpiperazine-2-methanethiols, and 2,2-dimethyl-3-(chloromethyl)thiirane does not react at all. The behavior of epihalohydrins in reaction with the N,N′-dimethylethylenediamine is similar to that of their thioanalogs. The specific features of these reactions are discussed from the viewpoint of the known competition between the intramolecular cyclization and nucleophilic opening of the cycle in unsymmetrically substituted thiiranes (oxiranes).
3-arylcarbonyl-1-(C-attached-N-heteryl)-1H-indoles
-
, (2008/06/13)
2-R2 -R4 -substituted-3-R3 -CO-1-[(C-attached-N-herteryl)-(Alk)n ]-1H-indoles useful as analgesic, anti-rheumatic, anti-inflammatory or anti-glaucoma agents.
