18420-41-2 Usage
Description
2-(CHLOROMETHYL)TETRAHYDROPYRAN, also known as 2-(Chloromethyl)tetrahydro-2H-pyran, is an organic compound that serves as a valuable reagent in the field of organic synthesis and chemical industry. It is characterized by its chloromethyl group attached to a tetrahydro-2H-pyran ring, which provides unique chemical properties and reactivity.
Uses
Used in Organic Synthesis Studies:
2-(CHLOROMETHYL)TETRAHYDROPYRAN is used as a reagent for organic synthesis studies due to its unique chemical properties and reactivity. It can be employed in various chemical reactions to synthesize a wide range of organic compounds, contributing to the development of new molecules with potential applications in various fields.
Used in Chemical Industry:
In the chemical industry, 2-(CHLOROMETHYL)TETRAHYDROPYRAN is utilized as a reagent for the production of various chemicals and materials. Its versatility in chemical reactions allows it to be used in the synthesis of different compounds, which can be further processed or used as intermediates in the production of various industrial products.
Used in Pharmaceutical Research:
Although not explicitly mentioned in the provided materials, 2-(CHLOROMETHYL)TETRAHYDROPYRAN may also find applications in pharmaceutical research. Its unique chemical structure could potentially be exploited to develop new drugs or drug candidates, particularly in the areas of medicinal chemistry and drug design.
Check Digit Verification of cas no
The CAS Registry Mumber 18420-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,2 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18420-41:
(7*1)+(6*8)+(5*4)+(4*2)+(3*0)+(2*4)+(1*1)=92
92 % 10 = 2
So 18420-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO/c7-5-6-3-1-2-4-8-6/h6H,1-5H2
18420-41-2Relevant articles and documents
Chemoenzymatic Halocyclization of γ,δ-Unsaturated Carboxylic Acids and Alcohols
Younes, Sabry H. H.,Tieves, Florian,Lan, Dongming,Wang, Yonghua,Süss, Philipp,Brundiek, Henrike,Wever, Ron,Hollmann, Frank
, (2019/12/27)
A chemoenzymatic method for the halocyclization of unsaturated alcohols and acids by using the robust V-dependent chloroperoxidase from Curvularia inaequalis (CiVCPO) as catalyst has been developed for the in situ generation of hypohalites. A broad range of halolactones and cyclic haloethers are formed with excellent performance of the biocatalyst.
Synthesis and solid-state polymerization of a macrocyclic compound with two butadiyne units
Kikuchi, Kohei,Tatewaki, Yoko,Okada, Shuji
, p. 387 - 394 (2017/06/14)
A macrocyclic compound 1 with two butadiyne and four dodecyloxy-substituted benzamide moieties was successfully synthesized, and its ring structure was confirmed by the MALDI-TOF mass spectra and the 1HNMR spectra. Compound 1 showed two modifications depending on solvent for the solidification. Characteristic excitonic absorption bands of polydiacetylene were observed at around 500 nm for one of the modifications after UV irradiation. Quantitative conversion of butadiyne moieties to the corresponding polydiacetylene structure was confirmed by the Raman spectra.
Efficient synthesis of 8,11-dimethylene-bicyclo[5.3.1]undecan-2-one
Gu, Haining,Xu, Wei Ming,Kinstle, Thomas H.
, p. 6449 - 6451 (2007/10/03)
We report here, an effective methodology for the preparation of 8,11-dimethylene-bicyclo[5.3.1]undecan-2-one. The key steps in these reactions were chloromethylation, cationic-alkyne cyclization and anionic fragmentation sequence.
