6271-14-3 Usage
Description
(2,3-dimethylnaphthalen-1-yl)(phenyl)methanone, also known as 2,3-dimethylnaphthyl-phenyl-ketone, is a synthetic ketone compound with an aromatic structure that features both naphthalene and phenyl groups. It serves as a versatile building block in the synthesis of organic compounds and pharmaceuticals, and may also find applications in materials science and as a reagent in chemical reactions.
Uses
Used in Pharmaceutical Industry:
(2,3-dimethylnaphthalen-1-yl)(phenyl)methanone is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel drug molecules with potential therapeutic properties.
Used in Organic Synthesis:
As a building block, (2,3-dimethylnaphthalen-1-yl)(phenyl)methanone is used in the creation of diverse organic compounds, facilitating the formation of complex molecular structures for a wide range of applications.
Used in Materials Science:
(2,3-dimethylnaphthalen-1-yl)(phenyl)methanone may be utilized in the development of new materials, potentially enhancing their properties or contributing to the creation of innovative material types.
Used as a Chemical Reaction Reagent:
(2,3-dimethylnaphthalen-1-yl)(phenyl)methanone can be employed as a reagent in various chemical reactions, aiding in the synthesis process and enabling the production of desired products with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 6271-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6271-14:
(6*6)+(5*2)+(4*7)+(3*1)+(2*1)+(1*4)=83
83 % 10 = 3
So 6271-14-3 is a valid CAS Registry Number.
6271-14-3Relevant articles and documents
A Cascade Approach to Naphthalene Derivatives from o-Alkynylbenzaldehydes and Enolizable Ketones via in-situ-Formed Acetals
Manojveer, Seetharaman,Balamurugan, Rengarajan
, p. 4254 - 4260 (2015/06/30)
Using the in-situ-formed acetal strategy, a facile approach has been developed to synthesize naphthalene derivatives from o-alkynylbenzaldehydes and enolizable ketones. In situ acetal formation assists the condensation between o-alkynylbenzaldehydes and enolizable ketones to give chalcone derivatives under Bronsted acidic conditions. In situ acetal formation facilitates the reaction by increasing the electrophilicity of the carbonyl carbon of the o-alkynylaldehyde through oxonium ion formation, and also by enhancing the nucleophilicity of the α carbon of the ketone through the formation of an enol ether. The formed chalcones undergo trans to cis isomerization to effect alkyne-carbonyl metathesis to give naphthalene derivatives.
