39689-04-8 Usage
Uses
Used in Organic Synthesis:
5-[(4-Chlorophenyl)sulfanyl]-2-furaldehyde is used as a building block in organic synthesis for the preparation of a variety of other compounds. Its unique structure with a furan ring and a chlorophenylsulfanyl substituent allows for the creation of diverse organic products.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-[(4-Chlorophenyl)sulfanyl]-2-furaldehyde is used as a key intermediate in the synthesis of potential drug candidates. Its chemical properties make it a valuable component in the development of new medications.
Used in Agrochemical Production:
5-[(4-Chlorophenyl)sulfanyl]-2-furaldehyde is also utilized in the agrochemical sector, where it serves as a starting material for the synthesis of various agrochemicals, contributing to the development of effective crop protection agents.
Used as a Sensory or Fragrance Agent:
Due to its aromatic properties, 5-[(4-Chlorophenyl)sulfanyl]-2-furaldehyde is used in the fragrance industry as a sensory or fragrance agent, adding unique scents to various products such as perfumes, cosmetics, and other consumer goods.
Used in Research and Development:
In the field of scientific research, 5-[(4-Chlorophenyl)sulfanyl]-2-furaldehyde is employed as a research compound for studying its chemical properties and potential applications in various chemical and material sciences.
Check Digit Verification of cas no
The CAS Registry Mumber 39689-04-8 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 39689-04:
(7*3)+(6*9)+(5*6)+(4*8)+(3*9)+(2*0)+(1*4)=168
168 % 10 = 8
So 39689-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H7ClO2S/c12-8-1-4-10(5-2-8)15-11-6-3-9(7-13)14-11/h1-7H
39689-04-8Relevant academic research and scientific papers
5-SUBSTITUTED 2-FURANCARBALDEHYDES AND WATER-SOLUBLE FURAN DERIVATIVES
Vegh, Daniel,Kovac, Jaroslav,Dandarova, Miroslava
, p. 961 - 966 (2007/10/02)
5-Halo-2-furaldehydes Ia, Ib react with trimethylamine in aprotic solvents to furnish 5-trimethylamonium salts of 2-furaldehyde IIa, IIb.The reactivity of this salt was utilized for a simple preparation of 5-substituted 2-furaldehydes IV in water at room temperature.The possibility to synthesize azomethines V and ethylenes VI, having the trimethylammonium group in position 5 of the furan ring maintained, is discussed.
