126522-01-8 Usage
Uses
Used in Medicinal Chemistry and Pharmaceuticals:
METHYL 4H-(1)-BENZOPYRANO(4 3-B)THIOPHE& is used as a potential therapeutic agent for various diseases due to its diverse biological activities, including antioxidant and anti-inflammatory properties. Its unique structure allows it to interact with biological targets, offering a promising avenue for the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, METHYL 4H-(1)-BENZOPYRANO(4 3-B)THIOPHE& is used as a building block or intermediate for the synthesis of more complex organic compounds. Its heterocyclic nature and the presence of a benzopyran ring fused with a thiophene ring make it a versatile component in the creation of novel organic molecules.
Used in Material Science:
METHYL 4H-(1)-BENZOPYRANO(4 3-B)THIOPHE& may also find applications in material science, where its unique structure and properties can be leveraged to develop new materials with specific characteristics. This could include the development of materials with enhanced electronic, optical, or mechanical properties, depending on the compound's interactions with other components in a material system.
Check Digit Verification of cas no
The CAS Registry Mumber 126522-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126522-01:
(8*1)+(7*2)+(6*6)+(5*5)+(4*2)+(3*2)+(2*0)+(1*1)=98
98 % 10 = 8
So 126522-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O3S/c1-15-13(14)11-6-8-7-16-10-5-3-2-4-9(10)12(8)17-11/h2-6H,7H2,1H3
126522-01-8Relevant academic research and scientific papers
Bogza, Yu. P.,Katsiel',Sharypova,Tolstikova,Fisyuk
, p. 1712 - 1718 (2015)
The formyl group of 4H-thieno[3,2-c]chromene-2-carbaldehyde was transformed into the respective nitrile, amide, ester, carboxylic, hydroxamic, or hydroxy group. Electrophilic substitution in 4H-thieno[3,2-c]chromene-2-carbaldehyde was shown to occur at the C-8 atom, while oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in methanol led to 4-methoxy-4H-thieno[3,2-c]chromene-2-carbaldehyde. The latter compound was found to possess high antiulcer activity.
4H-THIENO[3,2-C]CHROMENE-BASED INHIBITORS OF NOTUM PECTINACETYLESTERASE AND METHODS OF THEIR USE
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Page/Page column 22; 23, (2012/12/13)
Compounds that may be used to inhibit Notum Pectinacetylesterase are described, as well as compositions comprising them, and methods of their use to treat diseases and disorders affecting bone.
