71504-00-2 Usage
Description
1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is a chemical compound characterized by its molecular formula C11H11BrOS2. It is a yellowish crystalline solid with a molecular weight of 301.24 g/mol. 1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is known for its unique structure, which includes a bromo-phenyl group and a bis-methylsulfanyl group, endowing it with distinct properties and reactivity. Its composition and characteristics render it a versatile compound in various scientific and industrial applications.
Uses
Used in Organic Synthesis:
1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is utilized as a building block in organic synthesis, allowing the creation of more complex molecules. Its unique structure and reactivity make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is used as a key intermediate for the development of new drugs. Its unique properties and reactivity contribute to the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemicals:
1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE also finds application in the agrochemical sector, where it serves as a starting material for the synthesis of new agrochemicals. Its structure and properties enable the development of innovative products with improved performance in agriculture.
Used in Materials Science:
In the field of materials science, 1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is employed as a component in the development of advanced materials. Its unique properties and reactivity contribute to the creation of materials with enhanced characteristics for various applications, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 71504-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,0 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71504-00:
(7*7)+(6*1)+(5*5)+(4*0)+(3*4)+(2*0)+(1*0)=92
92 % 10 = 2
So 71504-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrOS2/c1-14-11(15-2)7-10(13)8-5-3-4-6-9(8)12/h3-7H,1-2H3
71504-00-2Relevant articles and documents
One-Pot Mitsunobu Protocol to Access Ketene S,S-/N,S-Acetals at Room Temperature
Saha, Priya,Ansari, Monish Arbaz,Shukla, Gaurav,Singh, Maya Shankar
supporting information, p. 5884 - 5888 (2021/11/27)
With unique chemical reactivity, α-oxoketene S,S- and N,S-acetals have attracted enormous attention in the past decades, whereas limited reports exist for their synthesis via eco-compatible protocols. Herein, we developed a one-pot protocol for symmetrical and unsymmetrical α-oxoketene S,S-/N,S-acetals through chemoselective alkylation of α-enolic dithioesters using Mitsunobu chemistry at room temperature. The operationally simple and user-friendly mild protocol tolerates a wide range of alcohols and α-enolic dithioesters/β-ketothioamides. Short reaction time, good yields, highly selective C?S functionalization, and E/Z-stereoselectivity are imperative characteristics of this strategy.
Bronsted acid catalyzed PhSe transfer versus radical aryl transfer: Linear codimerization of styrenes and internal olefins
Wu, Ping,Wang, Liandi,Wu, Kaikai,Yu, Zhengkun
supporting information, p. 868 - 871 (2015/03/30)
Bronsted acid p-TsOH·H2O-catalyzed hydrovinylation of styrenes with internal olefins α-oxo ketene dithioacetals was efficiently achieved in the presence of N-phenylselenophthalimide (N-PSP), regioselectively affording Markovnikov phenylselenati
