16547-34-5 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-dichloro-3-phenylcyclobut-2-en-1-one is used as a key intermediate for the synthesis of a variety of pharmaceuticals. Its unique structure allows it to be a versatile component in the creation of new medicinal compounds, contributing to the development of novel treatments and therapies.
Used in Agrochemical Production:
In the agrochemical industry, 2,4-dichloro-3-phenylcyclobut-2-en-1-one is utilized for the synthesis of various agrochemicals. Its application aids in the development of products designed to enhance crop protection and improve agricultural yields.
Used in Heterocyclic Compound Preparation:
2,4-dichloro-3-phenylcyclobut-2-en-1-one is used as a building block in the preparation of heterocyclic compounds. Its incorporation into these compounds is valuable for expanding the range of chemical structures available for various applications, including potential uses in material science and medicinal chemistry.
Used in Organic Chemical Research and Development:
As an important reagent in the field of chemical research and development, 2,4-dichloro-3-phenylcyclobut-2-en-1-one is employed in organic chemical synthesis. Its use in this context facilitates the exploration of new chemical reactions and the discovery of innovative synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 16547-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,4 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16547-34:
(7*1)+(6*6)+(5*5)+(4*4)+(3*7)+(2*3)+(1*4)=115
115 % 10 = 5
So 16547-34-5 is a valid CAS Registry Number.
16547-34-5Relevant academic research and scientific papers
The intermediacy of oxycyclobutenes in the synthesis and reactions of cyclobutenones and cyclobutenols
Frimer, Aryeh A.,Pizem, Hillel
, p. 12175 - 12186 (2007/10/03)
Vinylcyclobutenol 7, generated via the singlet oxygenation of alkylidenecyclobutene 5, rearranges at room temperature to a solvent dependent mixture of isomeric dienones 10 and 11. Alkylidenecyclobutene 5 was prepared in turn via an inverse Wittig additio
