954238-22-3 Usage
Uses
Used in Pharmaceutical Industry:
5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHEN-4-OL is used as a building block for the production of various types of drugs, including antiviral and antibacterial agents. It plays a crucial role in the development of medications that combat viral and bacterial infections.
Used in Agrochemical Industry:
5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHEN-4-OL is used as an intermediate in the synthesis of insecticides and herbicides. Its incorporation helps in creating effective pest control solutions for agricultural applications.
Used in Dye and Pigment Industry:
5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHEN-4-OL is used in the manufacturing of dyes and pigments. Its properties contribute to the creation of a wide range of colorants for various industries.
Used in Rubber and Plastic Additives Industry:
5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHEN-4-OL is utilized in the production of rubber and plastic additives. It enhances the performance and properties of these materials, making them more suitable for specific applications.
5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHEN-4-OL is of interest to researchers and manufacturers due to its versatile applications and potential for further development in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 954238-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,2,3 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 954238-22:
(8*9)+(7*5)+(6*4)+(5*2)+(4*3)+(3*8)+(2*2)+(1*2)=183
183 % 10 = 3
So 954238-22-3 is a valid CAS Registry Number.
954238-22-3Relevant academic research and scientific papers
MacHara, Ales,Svoboda, Jiri
, p. 59 - 65,7 (2013)
The reaction of propanedioic acid, 2-diazo-1,3-bis(1,1-dimethylethyl) ester (di-tert-butyl diazomalonate) with a series of cyclopenta[b]thiophenes in the presence of catalytic rhodium acetate was studied. The resulting SC ylides underwent a rearrangement to form a heterocycle with different topology; thialene, in very low yields. Experimental and spectral data for all compounds are provided.
