22408-41-9 Usage
Uses
Used in Chemical Synthesis:
2-VINYLOXYTETRAHYDROPYRAN is used as a key intermediate in the preparation of various complex organic molecules. Its unique structure allows for a range of reactions, including cycloadditions, oxidations, and reductions, making it a valuable building block in organic synthesis.
Used in Pharmaceutical Industry:
2-VINYLOXYTETRAHYDROPYRAN is used as a starting material for the synthesis of nucleotide phosphonate analogs, which are important antiviral agents. These analogs have shown potential in the treatment of viral infections, including HIV and hepatitis, by inhibiting viral replication and integration into the host genome.
Used in Catalyst Preparation:
2-VINYLOXYTETRAHYDROPYRAN is used as a precursor in the preparation of alkylidene molybdenum and tungsten compounds. These metal complexes are widely employed as catalysts in olefin metathesis reactions, which are essential in the production of various chemicals, polymers, and pharmaceuticals. The unique properties of 2-VINYLOXYTETRAHYDROPYRAN enable the formation of highly active and selective catalysts, contributing to the efficiency and versatility of these reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 22408-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,0 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22408-41:
(7*2)+(6*2)+(5*4)+(4*0)+(3*8)+(2*4)+(1*1)=79
79 % 10 = 9
So 22408-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-2-8-7-5-3-4-6-9-7/h2,7H,1,3-6H2
22408-41-9Relevant academic research and scientific papers
Triisobutylaluminum-Assisted Reductive Rearrangement of Alkyl 1-Alkenyl Acetals: An Easy Synthesis of β-Alkoxy Alcohols
Menicagli, R.,Malanga, C.,Dell'Innocenti, M.,Lardicci, L.
, p. 5700 - 5704 (2007/10/02)
Alkyl 1-alkenyl acetals react with Al-i-Bu3 to give very good yields of β-alkoxy alcohols through a reductive rearrangement.The reaction is totally regioselective, but no stereocontrol occurs.
