23717-59-1 Usage
Appearance
Yellow to orange crystalline solid The compound is a yellow to orange solid with a crystalline structure.
Solubility
Insoluble in water, soluble in organic solvents The compound does not dissolve in water but can dissolve in certain organic solvents, such as ethanol or acetone.
Uses
Dye, pharmaceutical synthesis, chemical intermediate 2,2-diphenyl-1H-indene-1,3(2H)-dione is used in the production of dyes, as a starting material for synthesizing pharmaceuticals, and as a chemical intermediate in various chemical reactions.
Reagent in organic chemistry
The compound serves as a reagent in organic chemistry reactions, aiding in the synthesis of other compounds or the study of reaction mechanisms.
Biological and pharmacological properties
The compound has been studied for its potential anti-inflammatory and anti-cancer properties, indicating possible applications in the medical field.
Wide range of applications
Due to its various uses and potential properties, 2,2-diphenyl-1H-indene-1,3(2H)-dione has a broad range of applications across different fields, including chemistry, pharmaceuticals, and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 23717-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,1 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23717-59:
(7*2)+(6*3)+(5*7)+(4*1)+(3*7)+(2*5)+(1*9)=111
111 % 10 = 1
So 23717-59-1 is a valid CAS Registry Number.
23717-59-1Relevant articles and documents
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Moubasher
, p. 3245 (1951)
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A new, efficient method for direct α-alkenylation of β-dicarbonyl compounds and phenols using alkenyltriarylbismuthonium salts
Matano, Yoshihiro,Imahori, Hiroshi
, p. 5505 - 5508 (2007/10/03)
Direct α-alkenylation of β-keto esters, β-diketone, and phenols with alkenyltriarylbismuthonium salts proceeded smoothly in the presence of 1,1,3,3-tetramethylguanidine to afford the corresponding α-alkenylated carbonyl compounds (β,γ-unsaturated carbonyl compounds) in good yields. The high leaving ability of the triarylbismuthonio group is a key driving force to achieve the C-C bond formation at the vinylic carbon under mild conditions.
A study on the friedel-crafts type reaction of ninhydrin with arenes
Song, Hyun Nam,Seong, Mi Ra,Son, Ji Suk,Kim, Jae Nyoung
, p. 1865 - 1870 (2007/10/03)
The reactions of ninhydrin (1, 1,2,3-indantrione) with arenes in the presence of concentrated sulfuric acid afforded mono- or di-substituted ninhydrin derivatives at the 2-position in reasonable yields.
