7712-05-2 Usage
Description
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is an organic compound characterized by a unique heterocyclic structure consisting of thiophene and thiophene-2-carboxylic acid moieties. It is a versatile intermediate in the synthesis of various organic and pharmaceutical compounds due to its chemical reactivity and structural properties.
Uses
Used in Organic Synthesis:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is used as an organic synthesis intermediate for the preparation of a wide range of chemical compounds. Its unique structure allows for various chemical reactions, such as substitution, addition, and condensation, enabling the synthesis of complex organic molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is used as a pharmaceutical intermediate in the development of new drugs and therapeutic agents. Its chemical properties make it a valuable building block for the synthesis of pharmaceutical compounds with potential applications in treating various diseases and medical conditions.
Used in Laboratory Research and Development:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is utilized in laboratory research and development processes to explore its chemical properties, reactivity, and potential applications in various fields. Researchers use this compound to investigate new synthetic routes, reaction mechanisms, and the development of novel chemical compounds with specific properties and functions.
Used in Chemical Production Processes:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is employed in chemical production processes to manufacture a variety of chemical products, including pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility as a synthetic intermediate allows for the efficient production of target compounds with desired properties and applications.
Synthesis
Compound 3 was dissolved in ethanol,Potassium hydroxide was added and refluxed at 78 ° C for 4 h,After cooling to room temperature (25 ° C), the reaction solution was extracted with IM HCl, extracted with ethyl acetate, dried over Mg2SO4 and dried to give the title compound 4 (92%).
Check Digit Verification of cas no
The CAS Registry Mumber 7712-05-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7712-05:
(6*7)+(5*7)+(4*1)+(3*2)+(2*0)+(1*5)=92
92 % 10 = 2
So 7712-05-2 is a valid CAS Registry Number.
