39689-03-7 Usage
Uses
Used in Organic Synthesis:
5-(PHENYLSULFANYL)-2-FURALDEHYDE is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for versatile reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-(PHENYLSULFANYL)-2-FURALDEHYDE is used as a precursor in the development of new drugs. Its chemical properties enable the creation of novel therapeutic agents that can target specific biological pathways, potentially leading to the discovery of innovative treatments for various diseases.
Used in Agrochemical Development:
5-(PHENYLSULFANYL)-2-FURALDEHYDE also finds application in the agrochemical sector, where it is used in the synthesis of new pesticides and other agricultural chemicals. Its potential to form stable and effective compounds makes it a promising candidate for improving crop protection and yield.
Used in Research and Development:
Due to its unique chemical structure and properties, 5-(PHENYLSULFANYL)-2-FURALDEHYDE is utilized in research and development laboratories to explore its potential applications and understand its chemical behavior. This helps in advancing the knowledge of organic chemistry and contributes to the development of new technologies and products.
Check Digit Verification of cas no
The CAS Registry Mumber 39689-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,8 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39689-03:
(7*3)+(6*9)+(5*6)+(4*8)+(3*9)+(2*0)+(1*3)=167
167 % 10 = 7
So 39689-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O2S/c12-8-9-6-7-11(13-9)14-10-4-2-1-3-5-10/h1-8H
39689-03-7Relevant academic research and scientific papers
Copper-Catalyzed Electrophilic Thiolation of Organozinc Halides by Using N-Thiophthalimides Leading to Polyfunctional Thioethers
Gra?l, Simon,Hamze, Clémence,Koller, Thadd?us J.,Knochel, Paul
supporting information, p. 3752 - 3755 (2019/02/13)
(Hetero)aryl, benzylic, and alkyl zinc halides were thiolated with N-thiophthalimides at 25 °C within 1 h in the presence of 5–10 % Cu(OAc)2?H2O to furnish the corresponding polyfunctionalized thioethers in good yields. This electrop
Application of furyl-stabilized sulfur ylides to a concise synthesis of 8a-epi-swainsonine
Bi, Jie,Aggarwal, Varinder K.
, p. 120 - 122 (2008/09/19)
The total synthesis of 8a-epi-swainsonine has been achieved in 20% overall yield from R-glyceraldehyde dimethylacetonide 3 through epoxidation with the achiral furyl-substituted sulfonium ylide 2d as one of the key steps. The Royal Society of Chemistry.
Synthesis of sulfone-substituted furan chromophores with high molecular hyperppolarizability
Chou, Shang-Shing P.,Shen, Chih-Hung
, p. 6407 - 6410 (2007/10/03)
A series of sulfone-substituted furan chromophores were synthesized which showed high molecular hyperpolarizabilities as measured by solvatochromism, and good transparency in the visible region.
