17078-41-0 Usage
Uses
Used in Organic Synthesis:
2,4-dibenzylidenecyclobutanone is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of complex organic molecules for pharmaceutical, chemical, and material applications.
Used in Material Science:
In the field of material science, 2,4-dibenzylidenecyclobutanone is employed as a precursor for developing new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of novel substances with enhanced characteristics, such as improved stability, reactivity, or selectivity.
Used in Pharmaceutical Research:
2,4-dibenzylidenecyclobutanone is studied for its potential as an anti-cancer agent. Its biological activities are of interest to researchers who aim to develop new therapeutic agents for the treatment of various types of cancer. 2,4-dibenzylidenecyclobutanone's ability to interact with biological targets and modulate cellular processes makes it a promising candidate for further investigation and development in oncology.
Used in Drug Delivery Systems:
2,4-dibenzylidenecyclobutanone may also be utilized in the design of drug delivery systems. Its structural features can be leveraged to improve the solubility, bioavailability, and targeted delivery of therapeutic agents, thereby enhancing their efficacy and reducing side effects in medical treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 17078-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,7 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17078-41:
(7*1)+(6*7)+(5*0)+(4*7)+(3*8)+(2*4)+(1*1)=110
110 % 10 = 0
So 17078-41-0 is a valid CAS Registry Number.
17078-41-0Relevant academic research and scientific papers
The synthesis and chlorosulfonation of some diarylidene and heteroarylidene ketones with varying alicyclic ring size
Cremlyn, Richard J.,Frearson, Martin J.,Graham, Stephen
, p. 205 - 218 (2007/10/03)
A series of diarylidene and heteroarylidene ketones (1-20) was prepared using alicyclic ketones ((CH2)nC=O where n=3 to 7).An improved synthesis of 2,4-dibenzylidenecyclobutanone (1) is described and the ease of preparation of the arylidene derivatives is considered in terms of the size of the alicyclic ring.Treatment of 2,5-dibenzylidenecyclopentanone (2) with chlorosulfonic acid (10 mole equivalents) afforded the 4,4'-bis-sulfonyl chloride (23), reducing the amount of chlorosulfonis acid (6 mole equivalents) produced the corresponding mono-sulfonyl chloride (24).Only the respective 4,4'-bis-sulfonyl chlorides (39, 45, 51) could be isolated from the diarylidene ketones derived from larger alicyclic rings.Attempted chlorosulfonation of 2,4-dibenzylidene cyclobutanone (1) gave a mixture of products which could not be clearly characterised.The sulfonyl chlorides were converted into stable sulfonamides (25-29, 35, 36, 38, 40-44, 46-48, 52, 54) by condensation with amines, and selected samples were screened for biological activity as potential insecticides, herbicides, and fungicides.The orientation of sulfonation is discussed in relation to stereoelectronic factors and the relevant spectral data.Key words: Arylidene and heteroarylidene ketones, chlorosulfonation, sulfonamides
