321744-15-4 Usage
Uses
Used in Pharmaceutical Industry:
(2S)-2-([tert-butyl(dimethyl)silyl]oxymethyl)-2,3-dihydro-1H-indole is used as an intermediate in the synthesis of various pharmaceutical compounds. Its protected indole structure allows for the development of new drugs with specific therapeutic properties, potentially leading to advancements in the treatment of various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, (2S)-2-([tert-butyl(dimethyl)silyl]oxymethyl)-2,3-dihydro-1H-indole serves as a key component in the creation of novel agrochemicals. Its unique structure can be utilized to develop pesticides, herbicides, or other agricultural chemicals that can improve crop yields and protect plants from pests and diseases.
Used in Material Sciences:
(2S)-2-([tert-butyl(dimethyl)silyl]oxymethyl)-2,3-dihydro-1H-indole is employed in material sciences for the development of new materials with specific properties. Its chemical structure can be manipulated to create materials with tailored characteristics, such as improved stability, reactivity, or other desirable traits, for use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 321744-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,7,4 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 321744-15:
(8*3)+(7*2)+(6*1)+(5*7)+(4*4)+(3*4)+(2*1)+(1*5)=114
114 % 10 = 4
So 321744-15-4 is a valid CAS Registry Number.
321744-15-4Relevant articles and documents
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.
