85895-83-6 Usage
Description
3,5-dimethylthiophene-2-carbaldehyde is a chemical compound characterized by the molecular formula C9H10OS. It presents itself as a yellow to light brown liquid, accompanied by a strong, foul odor. 3,5-dimethylthiophene-2-carbaldehyde is distinguished by its unique chemical and physical properties, which lend it to a variety of applications across different industries.
Uses
Used in Flavor and Fragrance Industry:
3,5-dimethylthiophene-2-carbaldehyde serves as a crucial fragrance and flavoring agent, specifically in the production of food and cosmetic products. Its distinct aromatic profile contributes to the creation of desirable scents and tastes, enhancing the sensory experience of these consumer goods.
Used in Pharmaceutical Synthesis:
In the pharmaceutical sector, 3,5-dimethylthiophene-2-carbaldehyde operates as an intermediate in the synthesis of various drugs. Its chemical structure allows for its incorporation into medicinal compounds, potentially leading to the development of new therapeutic agents.
Used in Agrochemical Production:
Similarly, this compound is utilized as an intermediate in the synthesis of agrochemicals. Its role in this industry is instrumental in developing products that can protect crops and enhance agricultural yields.
Used in Organic Synthesis and Materials Science:
3,5-dimethylthiophene-2-carbaldehyde also holds potential in the realms of organic synthesis and materials science. Its unique properties make it a valuable component in the development of new materials and chemical processes.
However, it is imperative to exercise caution when handling 3,5-dimethylthiophene-2-carbaldehyde, as it is classified as flammable and can cause skin and eye irritation upon contact. Proper safety measures should be implemented to mitigate these risks.
Check Digit Verification of cas no
The CAS Registry Mumber 85895-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85895-83:
(7*8)+(6*5)+(5*8)+(4*9)+(3*5)+(2*8)+(1*3)=196
196 % 10 = 6
So 85895-83-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8OS/c1-5-3-6(2)9-7(5)4-8/h3-4H,1-2H3
85895-83-6Relevant articles and documents
Synthesis and photochromic properties of tetrakis(3,5-dimethyl-2-thienyl)- and tetrakis(2,5-dimethyl-3-thienyl)ethylenes
Belen'kii,Gromova,Kolotaev,Nabatov,Krayushkin
, p. 1208 - 1213 (2007/10/03)
Tetrakis(3,5-dimethyl-2-thienyl)ethylene and tetrakis(2,5-dimethyl-3- thienyl)ethylene were obtained from the corresponding dithienyl ketones by the McMurry reaction. The photochromic properties of the compounds obtained were studied.
A Thiophene Analogue of Praziquantel, and Related Systems, by Intramolecular Cyclisation of Acyliminium Salts
Meth-Cohn, Otto,Vij, Rup Rani,Smalley, Robert K.,Bass, Robert J.
, p. 1001 - 1018 (2007/10/02)
N--succinimide (7a) and -glutarimide (7b) on reduction with sodium borohydride in methanol at -10 deg C yield the respective hydroxylactams which on treatment with formic acid cyclise via the intermediate acyliminium ions to 4,5,9,9a-tetrahydropyrrolothienopyridin-7-one (9a) and 4,5,8,9,10,10a-hexahydropyridothienopyridin-7-one (9b) respectively.In a similar manner, 4-cyclohexylcarbonyl-1-piperazine-2,6-dione (11) is converted into the thiophene isostere (2) of praziquantel (1).Likewise, formic acid induced cyclisations of the hydroxylactams derived from N-- (16) and N-succinimide (19) furnish 5,6,10,10a-tetrahydropyrrolothienothiazepin-8(9H)-one (18) and 5,6,10,10a-tetrahydropyrrolothienothiazepin-8(9H)-one (21), respectively.
