94460-78-3 Usage
Uses
Used in Pharmaceutical Development:
2,3-dimethyl-1-(phenylsulfonyl)-2,3-dihydro-1H-indole is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique molecular structure and potential biological activities make it a candidate for various therapeutic applications, including the treatment of diseases and disorders.
Used in Agrochemical Development:
In the agrochemical industry, 2,3-dimethyl-1-(phenylsulfonyl)-2,3-dihydro-1H-indole is used as a potential component in the formulation of new pesticides or herbicides. Its specific molecular features may contribute to the effectiveness of these products in controlling pests and weeds, thereby enhancing crop protection and yield.
Further Research:
2,3-dimethyl-1-(phenylsulfonyl)-2,3-dihydro-1H-indole is used in scientific research to explore its chemical properties, biological activities, and potential applications. Ongoing studies aim to understand its interactions with biological systems and its efficacy in various applications, which could lead to the discovery of new uses and formulations in both the pharmaceutical and agrochemical sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 94460-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,4,6 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94460-78:
(7*9)+(6*4)+(5*4)+(4*6)+(3*0)+(2*7)+(1*8)=153
153 % 10 = 3
So 94460-78-3 is a valid CAS Registry Number.
94460-78-3Relevant academic research and scientific papers
Manganese(III) acetate oxidation of alkyl substituted 1- (phenylsulfonyl)indoles
Ketcha,Zhou,Grossie
, p. 565 - 574 (2007/10/02)
Methyl substituted 1-(phenylsulfonyl)indoles undergo tandem oxidation of the indoline ring and a C-2 methyl group. If there is no alkyl substituent at the C-2 position, nuclear acetoxylation can occur to afford oxindoles.
THE REDUCTION OF N-(PHENYLSULFONYL)INDOLES WITH SODIUM CYANOBOROHYDRIDE IN TRIFLUOROACETIC ACID
Ketcha, Daniel M.,Lieurance, Brett A.
, p. 6833 - 6836 (2007/10/02)
The reduction of N-(phenylsulfonyl)indoles to the corresponding N-(phenylsulfonyl)indolines can be accomplished with good to excellent yields using cyanoborohydride (NaCNBH3) in trifluoroacetic acid (TFA).
