180987-85-3 Usage
Uses
Used in Organic Synthesis:
Dihydro-5-(1-naphthalenyl)-2-furanone is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different functional groups and properties, making it a versatile building block in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Dihydro-5-(1-naphthalenyl)-2-furanone is used as a key component in the development of new drugs. Its chemical structure can be modified to create potential drug candidates with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
Dihydro-5-(1-naphthalenyl)-2-furanone is also employed in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic routes. Its unique structure provides researchers with valuable insights into the reactivity and behavior of similar compounds, furthering the understanding of organic chemistry.
Used in Material Science:
In the field of material science, Dihydro-5-(1-naphthalenyl)-2-furanone can be used to develop novel materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with enhanced characteristics, such as improved stability, solubility, or conductivity.
Check Digit Verification of cas no
The CAS Registry Mumber 180987-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,9,8 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 180987-85:
(8*1)+(7*8)+(6*0)+(5*9)+(4*8)+(3*7)+(2*8)+(1*5)=183
183 % 10 = 3
So 180987-85-3 is a valid CAS Registry Number.
180987-85-3Relevant academic research and scientific papers
One-Pot γ-Lactonization of Homopropargyl Alcohols via Intramolecular Ketene Trapping
Yamane, Daichi,Tanaka, Haruna,Hirata, Akihiro,Tamura, Yumiko,Takahashi, Daichi,Takahashi, Yusuke,Nagamitsu, Tohru,Ohtawa, Masaki
, p. 2831 - 2835 (2021/05/05)
A one-pot γ-lactonization of homopropargyl alcohols via an alkyne deprotonation/boronation/oxidation sequence has been developed. Oxidation of the generated alkynyl boronate affords the corresponding ketene intermediate, which is trapped by the adjacent hydroxy group to furnish the γ-lactone. We have optimized the conditions as well as examined the substrate scope and synthetic applications of this efficient one-pot lactonization.
Indium-Catalyzed Direct Conversion of Lactones into Thiolactones and Selenolactones in the Presence of Elemental Sulfur and Selenium
Sakai, Norio,Horikawa, Shuhei,Ogiwara, Yohei
, p. 565 - 574 (2017/12/26)
The direct conversion of lactones into thiolactones with elemental sulfur (S 8) catalyzed by InCl 3 /PhSiH 3 in a one-pot reaction is described. This catalytic system was successfully applied to the novel preparation of selenolactones from lactones and selenium.
Gallium-catalyzed reductive lactonization of γ-keto acids with a hydrosilane
Sakai, Norio,Horikawa, Shuhei,Ogiwara, Yohei
, p. 81763 - 81766 (2016/09/09)
Described herein is the GaCl3-catalyzed lactonization of γ-keto carboxylic acids in the presence of PhSiH3 leading to the direct preparation of γ-lactone derivatives. This reducing system showed a relatively wide functional group tolerance.
