223575-76-6 Usage
Uses
Used in Pharmaceutical Industry:
2'-Chloro-biphenyl-2-carbaldehyde is used as a chemical intermediate for the synthesis of active pharmaceutical ingredients. Its reactivity and structural features contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2'-Chloro-biphenyl-2-carbaldehyde is employed as a building block in the creation of active ingredients for pesticides, enhancing the effectiveness of these products in agricultural settings.
Used in Dye Manufacturing:
2'-CHLORO-BIPHENYL-2-CARBALDEHYDE is utilized in the production of dyes, where its chemical properties allow for the creation of a range of colorants used in various industries.
Used in Fragrance Production:
2'-Chloro-biphenyl-2-carbaldehyde is also used in the manufacture of fragrances, capitalizing on its ability to contribute to the scent profiles of various products.
Used in Specialty Chemicals:
Its unique properties make 2'-Chloro-biphenyl-2-carbaldehyde a valuable component in the development of specialty chemicals for specific industrial applications.
Used in Research and Development:
Due to its unique chemical properties and reactivity, 2'-Chloro-biphenyl-2-carbaldehyde may be employed in research and development initiatives aimed at discovering new chemical reactions or creating novel compounds with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 223575-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,7 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 223575-76:
(8*2)+(7*2)+(6*3)+(5*5)+(4*7)+(3*5)+(2*7)+(1*6)=136
136 % 10 = 6
So 223575-76-6 is a valid CAS Registry Number.
223575-76-6Relevant academic research and scientific papers
Gold Catalysts Can Generate Nitrone Intermediates from a Nitrosoarene/Alkene Mixture, Enabling Two Distinct Catalytic Reactions: A Nitroso-Activated Cycloheptatriene/Benzylidene Rearrangement
Cheng, Mu-Jeng,Kardile, Rahul Dadabhau,Kuo, Tung-Chun,Liu, Rai-Shung,More, Sayaji Arjun
, p. 5506 - 5511 (2021/07/31)
Gold-catalyzed reactions of cycloheptatrienes with nitrosoarenes yield nitrone derivatives efficiently. This reaction sequence enables us to develop gold-catalyzed aerobic oxidations of cycloheptatrienes to afford benzaldehyde derivatives using CuCl and nitrosoarenes as co-catalysts (10-30 mol %). Our density functional theory calculations support a novel nitroso-activated rearrangement, tropylium → benzylidene. With the same nitrosoarenes, we developed their gold-catalyzed [2 + 2 + 1]-annulations between nitrosobenzene and two enol ethers to yield 5-alkoxyisoxazolidines using 1,4-cyclohexadienes as hydrogen donors.
