148344-52-9 Usage
Uses
Used in Organic Synthesis:
2-(2-(bromomethyl)phenoxy)tetrahydro-2H-pyran is utilized as a versatile building block in organic synthesis for the creation of complex organic molecules. The presence of the bromine atom in the molecule allows for a variety of reactions, such as substitution and coupling, which are crucial for the development of new chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(2-(bromomethyl)phenoxy)tetrahydro-2H-pyran is employed as a key intermediate in the preparation of biologically active compounds. Its unique structure and reactivity make it a valuable component in the synthesis of drugs with potential therapeutic applications.
Used in Materials Science:
2-(2-(bromomethyl)phenoxy)tetrahydro-2H-pyran may also find applications in the field of materials science, where its structural and chemical properties could contribute to the development of new materials with specific properties for various uses.
Used in Drug Development:
2-(2-(bromomethyl)phenoxy)tetrahydro-2H-pyran has potential applications in drug development, where it could be used to create new pharmaceuticals with novel mechanisms of action. Its reactivity and structural features make it a promising candidate for the design and synthesis of innovative drug molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 148344-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148344-52:
(8*1)+(7*4)+(6*8)+(5*3)+(4*4)+(3*4)+(2*5)+(1*2)=139
139 % 10 = 9
So 148344-52-9 is a valid CAS Registry Number.
148344-52-9Relevant academic research and scientific papers
One Pot Synthesis of Polycyclic Oxygen Aromatics. Part IV. Reaction of THP Ether of 2-Bromomethyl Phenols
Kasturi, Tirumalai R.,Mandal, Asish B.,Sumana, Bangalore G.,Rajasekhar, Betagiri
, p. 2751 - 2760 (2007/10/02)
Reaction of 2-bromomethyl-1-(2'-tetrahydropyranyloxy)benzene 3a with tetrachlorocatechol (TCC) in acetone in presence of anhydrous K2CO3 resulted in the formation of diastereomeric products to which cis- and trans- 6-chloro-8-hydroxy-8-(2-oxopropyl)spiroxanthen-9,2'(1'H)benzofuran>-7(8H)-one (7a and 8a) structures were assigned, along with tetrachlorocatechol ethers (5a and 6a).Similar reaction of 3a with tetrabromocatechol (TBC) gave the expected monobromo compounds 7d and 8d along with the ethers 5d and 6d.When the reaction was repeated with substrates 3b-c with TCC/TBC in ketonic solvents (acetone/methyl ethyl ketone), the corresponding compounds 5b-c to 8b-c, 5e-f to 6e-f, 7e-g and 8e-h were obtained.A suitable explanation has been given for the formation of acetonyl compound 6 in this reaction.
