19956-53-7 Usage
Uses
Used in Pharmaceutical Industry:
2-[(1Z,2E)-1-Hydroxy-3-phenyl-2-propenylidene]-4-methoxy-4-cyclopentene-1,3-dione is used as a potential pharmaceutical compound for its unique chemical structure, which may offer novel therapeutic properties. Its hydroxyphenylpropenylidene and methoxy groups could interact with biological targets, providing new avenues for drug development.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2-[(1Z,2E)-1-Hydroxy-3-phenyl-2-propenylidene]-4-methoxy-4-cyclopentene-1,3-dione serves as a reagent due to its enone functionality. Its double bond adjacent to the carbonyl group allows for various chemical reactions, enabling the synthesis of new compounds with potential applications in different fields.
Further research is necessary to fully understand the properties and potential uses of 2-[(1Z,2E)-1-Hydroxy-3-phenyl-2-propenylidene]-4-methoxy-4-cyclopentene-1,3-dione, as its complex structure and unique features may unlock new opportunities in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19956-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,5 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19956-53:
(7*1)+(6*9)+(5*9)+(4*5)+(3*6)+(2*5)+(1*3)=157
157 % 10 = 7
So 19956-53-7 is a valid CAS Registry Number.
19956-53-7Relevant academic research and scientific papers
Formal synthesis of linderone and lucidone based on one-pot cyclizations of 1,3-bis-silyl enol ethers with oxalyl chloride
Bose, Gopal,Langer, Peter
, p. 1021 - 1023 (2007/10/03)
A formal synthesis of the acylcyclopentenediones linderone and lucidone is reported which is based on the cyclization of 2,4-bis(trimethylsilyloxy)-1,3,5- hexatrienes with oxalyl chloride and on the synthesis and functionalization of γ-(2-silyloxypropenyl
Synthesis of Lucidones
Lee, Hiok-Huang,Que, Yoon-Ten,Ng, Soon
, p. 453 - 456 (2007/10/02)
Reaction of 2-cinnamoyl-3-hydroxy-5-methoxy-1,4-benzoquinone (10) with acetic anhydride-dimethyl sulphoxide yielded (E)-4-(cinnamoylmethylene)-2-methoxybut-2-en-4-olide (4).Assignment of configuration of the exocyclic double bond in (4) is based on compar