33898-90-7 Usage
Description
2-Thenoylacetonitrile, with the CAS number 33898-90-7, is a white to light yellow crystal powder that serves as a versatile compound in the realm of organic synthesis. Its unique chemical structure allows it to be a valuable building block for the creation of various complex organic molecules.
Uses
Used in Pharmaceutical Industry:
2-Thenoylacetonitrile is used as an intermediate in the synthesis of pharmaceutical compounds. Its chemical properties make it suitable for the development of new drugs, particularly those targeting specific medical conditions.
Used in Chemical Industry:
In the chemical industry, 2-Thenoylacetonitrile is used as a key component in the production of various organic chemicals. Its versatility in organic synthesis allows for the creation of a wide range of products, from dyes to agrochemicals.
Used in Research and Development:
2-Thenoylacetonitrile is also utilized in research and development settings, where it can be employed to study the properties and reactions of different organic compounds. This helps scientists and researchers to better understand the behavior of various molecules and develop new applications for them.
Overall, 2-Thenoylacetonitrile is a valuable compound with a diverse range of applications across different industries, including pharmaceuticals, chemical production, and research and development. Its unique properties and versatility in organic synthesis make it an essential tool for the creation of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 33898-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,8,9 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33898-90:
(7*3)+(6*3)+(5*8)+(4*9)+(3*8)+(2*9)+(1*0)=157
157 % 10 = 7
So 33898-90-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NOS/c8-4-3-6(9)7-2-1-5-10-7/h1-2,5H,3H2
33898-90-7Relevant articles and documents
Pyrolytic behavior of substituted N-aminoheteroaromatics: Synthesis of pyrazolo[1,5-a]pyridine and 3-substituted 3-oxo-propionitrile derivatives
Al-Awadi, Nouria A.,Abdelkhalik, Mervat,Patel, Mehul,Dib, Hicham H.
, p. 989 - 992 (2008/03/29)
(Chemical Equation Presented) Flash vacuum pyrolysis (FVP) of 1,7-bis-(3-aroylideneamino)-4,6,10,12-tetramethyl-2,8-dioxo-1, 7-diazacyclododeca-3,5,9,11-tetraene-3,9-dicarbonitriles 11a-c at 650°C and 0.02 Torr yielded 5,7-dimethyl-3-(4-methylbenzoyl)-pyrazolo[1,5-a]pyridine-4- carbonitrile 14, 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile 16 and 3-aryl-3-oxo-propionitriles 17a,b. A plausible mechanism is suggested to account for the formation of the products.
