10276-90-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,3-dimethyl-2,3-dihydro-1H-indole is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs and pesticides.
Used in Organic Electronics:
2,3-dimethyl-2,3-dihydro-1H-indole has been studied for its potential applications in the field of organic electronics. Its electronic properties, such as charge transport and stability, make it a promising candidate for use in organic semiconductors and other electronic devices.
Used in Fragrance and Flavoring Industries:
2,3-dimethyl-2,3-dihydro-1H-indole is also used as a component in the production of fragrances and flavorings. Its unique chemical structure contributes to the creation of distinct scents and tastes, making it valuable in the development of new fragrances and flavor compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 10276-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10276-90:
(7*1)+(6*0)+(5*2)+(4*7)+(3*6)+(2*9)+(1*0)=81
81 % 10 = 1
So 10276-90-1 is a valid CAS Registry Number.
10276-90-1Relevant academic research and scientific papers
Kinetic Resolution of 2-Substituted Indolines by N-Sulfonylation using an Atropisomeric 4-DMAP-N-oxide Organocatalyst
Murray, James I.,Flodén, Nils J.,Bauer, Adriano,Fessner, Nico D.,Dunklemann, Daniel L.,Bob-Egbe, Opetoritse,Rzepa, Henry S.,Bürgi, Thomas,Richardson, Jeffery,Spivey, Alan C.
supporting information, p. 5760 - 5764 (2017/05/12)
The first catalytic kinetic resolution by N-sulfonylation is described. 2-Substituted indolines are resolved (s=2.6–19) using an atropisomeric 4-dimethylaminopyridine-N-oxide (4-DMAP-N-oxide) organocatalyst. Use of 2-isopropyl-4-nitrophenylsulfonyl chloride is critical to the stereodiscrimination and enables facile deprotection of the sulfonamide products with thioglycolic acid. A qualitative model that accounts for the stereodiscrimination is proposed.
