27035-41-2 Usage
Uses
Used in Pharmaceutical Industry:
5-METHYL-1-BENZOTHIOPHENE-2-CARBALDEHYDE is used as a raw material for the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 5-METHYL-1-BENZOTHIOPHENE-2-CARBALDEHYDE is utilized as a starting material for the production of agrochemicals, aiding in the creation of pesticides and other agricultural chemicals.
Used in Flavor and Fragrance Industry:
5-METHYL-1-BENZOTHIOPHENE-2-CARBALDEHYDE is used as a flavor and fragrance ingredient in the production of perfumes, soaps, and other personal care products, enhancing their scent profiles.
Used in Specialty Chemicals and Functional Materials:
5-METHYL-1-BENZOTHIOPHENE-2-CARBALDEHYDE is employed as a building block in the creation of functional materials and specialty chemicals, contributing to the development of innovative products with unique properties.
Used in Research and Development:
5-METHYL-1-BENZOTHIOPHENE-2-CARBALDEHYDE is also utilized in research and development activities related to organic synthesis and chemical engineering, furthering scientific understanding and technological advancements in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 27035-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27035-41:
(7*2)+(6*7)+(5*0)+(4*3)+(3*5)+(2*4)+(1*1)=92
92 % 10 = 2
So 27035-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8OS/c1-7-2-3-10-8(4-7)5-9(6-11)12-10/h2-6H,1H3
27035-41-2Relevant academic research and scientific papers
Catalytic Deprotonative α-Formylation of Heteroarenes by an Amide Base Generated in Situ from Tetramethylammonium Fluoride and Tris(trimethylsilyl)amine
Shigeno, Masanori,Fujii, Yuki,Kajima, Akihisa,Nozawa-Kumada, Kanako,Kondo, Yoshinori
, p. 443 - 451 (2019/04/30)
Heteroarene formylations in DMF solution proceed in the presence of an amide base catalyst generated in situ from tetramethylammonium fluoride (TMAF) and tris(trimethylsilyl)amine (N(TMS)3). The reaction proceeds at room temperature and has an operationally simple procedure. Various heteroarenes, including benzothiophene, thiophene, benzothiazole, oxazole, and indole derivatives, can be formylated with high functional group tolerance.
