17514-66-8 Usage
Uses
Used in Pharmaceutical Industry:
5-CHLORO-3-METHYL-1H-BENZO[B]THIOPHENE-1,1-DIONE is used as a pharmaceutical agent for its antimicrobial, antifungal, and anti-inflammatory properties. Its diverse biological activities make it a promising candidate for the development of new drugs to combat various infections and inflammatory conditions.
Used in Agricultural Industry:
In the agricultural sector, 5-CHLORO-3-METHYL-1H-BENZO[B]THIOPHENE-1,1-DIONE is utilized as a bioactive compound with potential applications in crop protection and plant disease management. Its antimicrobial and antifungal properties can be harnessed to develop novel pesticides and fungicides, contributing to more sustainable and effective agricultural practices.
Used in Organic Synthesis:
5-CHLORO-3-METHYL-1H-BENZO[B]THIOPHENE-1,1-DIONE serves as a building block in organic synthesis, providing a foundation for the creation of more complex molecules with specific functions and properties. Its unique structure and reactivity make it a valuable component in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
While the precise uses and applications of 5-CHLORO-3-METHYL-1H-BENZO[B]THIOPHENE-1,1-DIONE are still being explored, its potential in various industries is evident. Further research is necessary to fully understand its chemical properties and unlock its full potential for practical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17514-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,1 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17514-66:
(7*1)+(6*7)+(5*5)+(4*1)+(3*4)+(2*6)+(1*6)=108
108 % 10 = 8
So 17514-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClO2S/c1-6-5-13(11,12)9-3-2-7(10)4-8(6)9/h2-5H,1H3
17514-66-8Relevant academic research and scientific papers
Enantioselective hydroarylation or hydroalkenylation of benzo[b]thiophene 1,1-dioxides with organoboranes
Hu, Fangdong,Jia, Jie,Li, Ximing,Xia, Ying
supporting information, p. 896 - 901 (2021/02/01)
An efficient protocol for the asymmetric hydroarylation and hydroalkenylation of benzo[b]thiophene 1,1-dioxides with organoboranes has been developed. The combination of a rhodium(I) precatalyst and a chiral diene ligand constitutes the catalytic system, which enables the facile synthesis of 2,3-dihydrobenzo[b]thiophene 1,1-dioxides in good yields with high enantioselectivities. The merging of this asymmetric hydroarylation with the downstream alkylations delivers 2,3-dihydrobenzo[b]thiophene 1,1-dioxides that contain two continuous quaternary stereocenters with high enantioselectivities in a diastereodivergent manner.
